Literature DB >> 6677410

[Genetic epidemiology of myotonic dystrophy in Kagoshima and Okinawa districts in Japan].

M Osame, T Furusho.   

Abstract

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Year:  1983        PMID: 6677410

Source DB:  PubMed          Journal:  Rinsho Shinkeigaku        ISSN: 0009-918X


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  5 in total

1.  The Change of Grip Strength in a Patient with Congenital Myotonic Dystrophy Over a 4-year Period.

Authors:  Shin Kikuchi; Naoki Kozuka; Eiji Uchida; Takafumi Ninomiya; Haruyuki Tatsumi; Hidekatsu Takeda; Nobutada Tachi
Journal:  J Jpn Phys Ther Assoc       Date:  2008

2.  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.

Authors:  H Yamagata; T Miki; M Nakagawa; K Johnson; R Deka; T Ogihara
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

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

Authors:  J Davies; H Yamagata; P Shelbourne; J Buxton; T Ogihara; P Nokelainen; M Nakagawa; R Williamson; K Johnson; T Miki
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

4.  Normal variation at the myotonic dystrophy locus in global human populations.

Authors:  C Zerylnick; A Torroni; S L Sherman; S T Warren
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

5.  Analysis of CTG repeat length variation in the DMPK gene in the general population and the molecular diagnosis of myotonic dystrophy type 1 in Malaysia.

Authors:  Kathlin K Ambrose; Taufik Ishak; Lay-Hoong Lian; Khean-Jin Goh; Kum-Thong Wong; Azlina Ahmad-Annuar; Meow-Keong Thong
Journal:  BMJ Open       Date:  2017-03-31       Impact factor: 2.692

  5 in total

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