Novel autosomal dominant TPM3 mutation causes a combined congenital fibre type disproportion-cap disease histological pattern

Saved in:
Bibliographic Details
Published in:Neuromuscular disorders : NMD 2022, Vol.32 (8), p.687-691
Main Authors: Bevilacqua, Jorge A, Contreras, Juan Pablo, Trangulao, Alejandra, Hernández, Úrsula, Brochier, Guy, Díaz, Jorge, Hughes, Ricardo, Campero, Mario, Romero, Norma B
Format: Report
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:1873-2364
DOI:10.1016/j.nmd.2022.05.014