Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy (Q37010363)
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scientific article published on 06 June 2013
Language | Label | Description | Also known as |
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English | Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy |
scientific article published on 06 June 2013 |
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Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy (English)
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Robert J Bryson-Richardson
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Haluk Topaloglu
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Richard J N Allcock
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Nigel F Clarke
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Francesco Muntoni
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Gianina Ravenscroft
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Satoko Miyatake
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Emily J Todd
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Pauliina Vornanen
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Kyle S Yau
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Yukiko K Hayashi
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Noriko Miyake
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Hiroshi Doi
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Hitoshi Osaka
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Sumimasa Yamashita
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Takashi Ohya
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Yuko Sakamoto
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Eriko Koshimizu
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Shintaro Imamura
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Michiaki Yamashita
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Kazuhiro Ogata
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Masaaki Shiina
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Ozge Ceyhan
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Lindsay C Swanson
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Norma B Romero
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Helge Amthor
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Nina Kresoje
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Padma Sivadorai
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Cathy Kiraly-Borri
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Goknur Haliloglu
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Beril Talim
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Diclehan Orhan
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Gulsev Kale
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Victoria A Fabian
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Mark R Davis
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Caroline A Sewry
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Adnan Manzur
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Yoram Nevo
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Ekkhard Willichowski
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Inger E Silberg
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Carina Wallgren-Pettersson
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Naomichi Matsumoto
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6 June 2013
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6-18
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