(Q70913393)

English

Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation

scientific article published on 01 February 1996

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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:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

myotonic dystrophy

1 reference

based on heuristic

inferred from title

author name string

H Yamagata

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

T Miki

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

M Nakagawa

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

K Johnson

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

R Deka

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

T Ogihara

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

publication date

1 February 1996

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

97

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

145-147

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

New founder haplotypes at the myotonic dystrophy locus in southern Africa.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophia myotonica in a Nigerian family

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anticipation in myotonic dystrophy: new light on an old problem

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic epidemiology of myotonic dystrophy in Kagoshima and Okinawa districts in Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo myotonic dystrophy mutation in a Nigerian kindred.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of the expansion mutation in myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of unstable DNA region in Japanese myotonic dystrophy patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/8566943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02265255

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8566943%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

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