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., Khan, A., Noor Ul Ayan, H., Budde, B., Altmüller, J., Korejo, A.A., Nürnberg, G., Thiele, H., Tariq, M., 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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