Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. [electronic resource]
- Brain : a journal of neurology Feb 2011
- 608-17 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1460-2156
10.1093/brain/awq374 doi
Adolescent Adult Aged Aged, 80 and over Arthrogryposis--genetics Charcot-Marie-Tooth Disease--genetics Child Female Hereditary Central Nervous System Demyelinating Diseases--genetics Hereditary Sensory and Motor Neuropathy--genetics Humans Male Middle Aged Mutation Myelin Proteins--genetics Phenotype Sural Nerve--pathology Transcription, Genetic