학술논문

O.08 Biallelic variants in the mitochondrial form of phosphoenolpyruvate carboxykinase (PCK2) cause a recessive form of Charcot-Marie-Tooth disease
Document Type
Abstract
Source
In Neuromuscular Disorders October 2022 32 Supplement 1:S93-S93
Subject
Language
ISSN
0960-8966