40478_2019_869_MOESM1_ESM.zip (79.02 MB)

MOESM1 of Bi-allelic mutations in uncoordinated mutant number-45 myosin chaperone B are a cause for congenital myopathy

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posted on 2019-12-19, 07:08 authored by Hormos Dafsari, Nur Kocaturk, Hülya-Sevcan Daimagüler, Anna Brunn, Jörg Dötsch, Joachim Weis, Martina Deckert, Sebahattin Cirak

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.

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Deutsche Forschungsgemeinschaft

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myopathological UNC 45B number -45 myosin chaperone B phenotypic findings isoform expression Figure S 2. Gene myopathy MOESM 1 UNC 45B variant uncoordinated disease model scheme electron Bi-allelic mutations tissue 1.

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