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Τρίτη 11 Οκτωβρίου 2022

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

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Journal of Human Genetics, Published online: 11 October 2022; doi:10.1038/s10038-022-01085-2

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