(Q28214725)

English

A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy

scientific article (publication date: 2002)

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

0 references

A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy (English)

0 references

dilated cardiomyopathy

1 reference

based on heuristic

inferred from title

author name string

Noboru Fujino

1

0 references

Masami Shimizu

2

0 references

Hidekazu Ino

3

0 references

Masato Yamaguchi

4

0 references

Toshihiko Yasuda

5

0 references

Mitsuru Nagata

6

0 references

Tetsuo Konno

7

0 references

Hiroshi Mabuchi

8

0 references

language of work or name

0 references

publication date

1 January 2002

0 references

American Journal of Cardiology

0 references

89

0 references

1

0 references

29-33

0 references

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

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%2801%2902158-0

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%2801%2902158-0

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%2801%2902158-0

7 January 2021

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Sudden death due to troponin T mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Occurrence and significance of progressive left ventricular wall thinning and relative cavity dilatation in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

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%2801%2902158-0

7 January 2021

Molecular cloning and developmental expression of human cardiac troponin T.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Patterns and significance of distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy. A wide angle, two dimensional echocardiographic study of 125 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: insights into disease pathogenesis and troponin function

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Angiotensin-I Converting Enzyme Genotypes and Left Ventricular Hypertrophy in Patients With Hypertrophic Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Sudden cardiac death in hypertrophic cardiomyopathy. Variability in phenotypic expression of beta-myosin heavy chain mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9149%2801%2902158-0

7 January 2021

Identifiers

10.1016/S0002-9149(01)02158-0

0 references

PubMed publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28214725&oldid=1517727049"