Literature DB >> 22258159

Myotonic dystrophy type 2 is rare in the Japanese population.

Tohru Matsuura, Narihiro Minami, Hajime Arahata, Kinji Ohno, Koji Abe, Yukiko K Hayashi, Ichizo Nishino.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2012        PMID： 22258159     DOI： 10.1038/jhg.2011.152

Source DB:  PubMed          Journal:  J Hum Genet        ISSN： 1434-5161            Impact factor:   3.172


× No keyword cloud information.
  4 in total

Review 1.  Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects.

Authors:  Giovanni Meola; Rosanna Cardani
Journal:  Neurol Sci       Date:  2017-01-11       Impact factor: 3.307

Review 2.  Biomolecular diagnosis of myotonic dystrophy type 2: a challenging approach.

Authors:  Giovanni Meola; Fiammetta Biasini; Rea Valaperta; Elena Costa; Rosanna Cardani
Journal:  J Neurol       Date:  2017-05-26       Impact factor: 4.849

Review 3.  Recent advances in myotonic dystrophy type 2.

Authors:  Christina M Ulane; Sarah Teed; Jacinda Sampson
Journal:  Curr Neurol Neurosci Rep       Date:  2014-02       Impact factor: 5.081

4.  Clinical and genetic analysis of the first known Asian family with myotonic dystrophy type 2.

Authors:  Takahiro Nakayama; Harumasa Nakamura; Yasushi Oya; Takashi Kimura; Ichiro Imahuku; Kinji Ohno; Ichizo Nishino; Koji Abe; Tohru Matsuura
Journal:  J Hum Genet       Date:  2014-01-16       Impact factor: 3.172
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.