Τρίτη 11 Οκτωβρίου 2022

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

alexandrossfakianakis shared this article with you from Inoreader

10038_2022_1085_Fig1_HTML.png

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
View on Web

Δεν υπάρχουν σχόλια:

Δημοσίευση σχολίου