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Journal description
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All issues of the corresponding volume
All articles of the corresponding issues
Details for article 16 of 23 found articles
| Title: |
Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy |
| Author: |
Ravenscroft, Gianina Miyatake, Satoko Lehtokari, Vilma-Lotta Todd, Emily J. Vornanen, Pauliina Yau, Kyle S. Hayashi, Yukiko K. Miyake, Noriko Tsurusaki, Yoshinori Doi, Hiroshi Saitsu, Hirotomo Osaka, Hitoshi Yamashita, Sumimasa Ohya, Takashi Sakamoto, Yuko Koshimizu, Eriko Imamura, Shintaro Yamashita, Michiaki Ogata, Kazuhiro Shiina, Masaaki Bryson-Richardson, Robert J. Vaz, Raquel Ceyhan, Ozge Brownstein, Catherine A. Swanson, Lindsay C. Monnot, Sophie Romero, Norma B. Amthor, Helge Kresoje, Nina Sivadorai, Padma Kiraly-Borri, Cathy Haliloglu, Goknur Talim, Beril Orhan, Diclehan Kale, Gulsev Charles, Adrian K. Fabian, Victoria A. Davis, Mark R. Lammens, Martin Sewry, Caroline A. Manzur, Adnan Muntoni, Francesco Clarke, Nigel F. North, Kathryn N. Bertini, Enrico Nevo, Yoram Willichowski, Ekkhard Silberg, Inger E. Topaloglu, Haluk Beggs, Alan H. Allcock, Richard J.N. Nishino, Ichizo Wallgren-Pettersson, Carina Matsumoto, Naomichi Laing, Nigel G. |
| Appeared in: |
The American journal of human genetics |
| Paging: | Volume 93 (2013) nr. 1 pages 13 p. |
| Year: |
2013 |
| Contents: | |
| Publisher: |
The American Society of Human Genetics |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 16 of 23 found articles
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