Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy-Reference-Cited by-同舟云学术

Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy

Published:2017-01 Issue:1 Volume:100 Page:169-178
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Miyatake Satoko,Mitsuhashi Satomi,Hayashi Yukiko K.,Purevjav Enkhsaikhan,Nishikawa Atsuko,Koshimizu Eriko,Suzuki Mikiya,Yatabe Kana,Tanaka Yuzo,Ogata Katsuhisa,Kuru Satoshi,Shiina Masaaki,Tsurusaki Yoshinori,Nakashima Mitsuko,Mizuguchi Takeshi,Miyake Noriko,Saitsu Hirotomo,Ogata Kazuhiro,Kawai Mitsuru,Towbin Jeffrey,Nonaka Ikuya,Nishino Ichizo,Matsumoto Naomichi

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference37 articles.

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4. Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy;Pelin;Proc. Natl. Acad. Sci. USA,1999

5. A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1;Laing;Nat. Genet.,1995

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