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Novel Form of Congenital Myopathy Caused by Biallelic Mutations in Uncoordinated Mutant Number-45 Myosin Chaperone B
Novel Form of Congenital Myopathy Caused by Biallelic Mutations in Uncoordinated Mutant Number-45 Myosin Chaperone B
2021
Sebahattin Cirak
Hülya-Sevcan Daimagüler
Federica Diofano
Hormos Salimi Dafsari
Anna Brunn
Joachim Weis
Martina Deckert
Peter Nürnberg
Steffen Just
Keywords:
Chaperone (protein)
Mutant
Medicine
Cell biology
Myosin
Congenital myopathy
Correction
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