A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family

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Item Type:	Letter
Title:	A novel MAP3K20 mutation causing centronuclear myopathy-6 with fiber-type disproportion in a Pakistani family
Creators Name:	Ahmad, I. and Khan, A. and Noor Ul Ayan, H. and Budde, B. and Altmüller, J. and Korejo, A.A. and Nürnberg, G. and Thiele, H. and Tariq, M. and Nürnberg, P. and Erdmann, J.
Keywords:	Skeletal Muscle, Mutation, Congenital Structural Myopathies, Pakistan
Source:	Journal of Human Genetics
ISSN:	1434-5161
Publisher:	Nature Publishing Group
Date:	11 October 2022
Official Publication:	https://doi.org/10.1038/s10038-022-01085-2
PubMed:	View item in PubMed

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