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Mutations in KLHL40 Are a Frequent Cause of Severe Autoso... | ResearchHub
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Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy
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Authors
Gianina Ravenscroft
54 more
Gianina Ravenscroft
•
Satoko Miyatake
52 more
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Nigel Laing
Published
June 6, 2013
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Journal
The American Journal of Human Genetics
Topics
Biology
Epidemiology
Medicine
Pathology
Cardiology And Cardiovascular Medicine
Show all topics
DOI
10.1016/j.ajhg.2013.05.004
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publisher-specific-oa
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Journal
The American Journal of Human Genetics
Topics
Biology
Epidemiology
Medicine
Pathology
Cardiology And Cardiovascular Medicine
Show all topics
DOI
10.1016/j.ajhg.2013.05.004
License
publisher-specific-oa
