MOESM1 of Bi-allelic mutations in uncoordinated mutant number-45 myosin chaperone B are a cause for congenital myopathy
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https://springernature.figshare.com/articles/MOESM1_of_Bi-allelic_mutations_in_uncoordinated_mutant_number-45_myosin_chaperone_B_are_a_cause_for_congenital_myopathy/11405898/1
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资源简介：
Additional file 1: Figure S1. Further myopathological, electron microscopical and phenotypic findings in our patient with UNC45B variant. Figure S2. Gene and isoform expression of UNC45B in various tissues and a possible disease model scheme.
提供机构：
figshare
创建时间：
2019-12-19
