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

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

by
Hormos Dafsari; Nur Kocaturk; Hülya-Sevcan Daimagüler; Anna Brunn; Jörg Dötsch; Joachim Weis; Martina Deckert; Sebahattin Cirak

Publication date
2019-12-19T07:08:20Z
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.
Addeddate
2021-12-17 22:09:49
Doi
10.6084/m9.figshare.11405898.v1
Identifier
springernature.figshare.com-11405898-v1
License
https://creativecommons.org/licenses/by/4.0/
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Internet Archive Python library 2.1.0
Source
https://springernature.figshare.com/articles/dataset/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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1

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