(Q77750556)

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Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family

scientific article published on 01 December 1998

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

familial hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

author name string

T H Hwang

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

W H Lee

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

A Kimura

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

M Satoh

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

T Nakamura

5

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

M K Kim

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

S K Choi

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

J E Park

8

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

publication date

1 December 1998

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

American Journal of Cardiology

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

82

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

12

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1509-1513

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Complete sequence and organization of the human cardiac beta-myosin heavy chain gene

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Structure of the actin-myosin complex and its implications for muscle contraction

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2898%2900695-X

7 January 2021

Identifiers

10.1016/S0002-9149(98)00695-X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9874056%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

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