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Dominant mutations in KBTBD13%252C a member of the BTB%252FK…

Dominant mutations in KBTBD13%252C a member of the BTB%252FKelch family%252C cause nemaline myopathy with cores.

Article, Chapter

Authors: N. Sambuughin

Publication: American Journal of Human Genetics, The, Volume:87, Issue:6

Published: Cell Press, 2010

ISSN: 0002-9297

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View Full Text Source:American Journal of Human Genetics, The,American Journal of Human Genetics, The,Elsevier ScienceDirect Journals Opens in new Window

Journal: American Journal of Human Genetics, The Source:Elsevier ScienceDirect Journals Opens in new Window

Collection: Elsevier ScienceDirect Journals Opens in new Window

Coverage:

1997-06~present; volume:60~present;issue:6~present

View Full Text Source:American Journal of Human Genetics, The,American Journal of Human Genetics, The,Cell Press Opens in new Window

Journal: American Journal of Human Genetics, The Source:Cell Press Opens in new Window

Collection: Cell Press Opens in new Window

Coverage:

1997-06~present; volume:60~present;issue:6~present

View Full Text Source:American Journal of Human Genetics,American Journal of Human Genetics,PubMed Central Opens in new Window

Journal: American Journal of Human Genetics Source:PubMed Central Opens in new Window

Collection: PubMed Central Opens in new Window

Coverage:

1949~6 months ago; volume:1~6 months ago

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