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Lev G Goldfarb

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American Journal of Human Genetics|November 27, 2010
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with coresNyamkhishig Sambuughin, Kyle S Yau, Montse Olivé, et al.
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Showing results (51-60 of 51) with videos related to

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Pageof 6
You have reached the last page of results.This site can display upto 51 results.
American Journal of Human Genetics|November 27, 2010
Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with coresNyamkhishig Sambuughin, Kyle S Yau, Montse Olivé, et al.
Pageof 6