| Literature DB >> 28914656 |
Nivedita U Jerath1, Michael E Shy.
Abstract
PURPOSE: Charcot-Marie-Tooth Disease type 1A (CMT1A) is caused by a duplication of the peripheral myelin protein gene 22 at chromosome 17p11.2-12. There is limited data regarding whether body mass index (BMI) affects electrophysiological or clinical data in those with CMT1A.Entities:
Mesh:
Year: 2017 PMID: 28914656 PMCID: PMC5679118 DOI: 10.1097/WNP.0000000000000415
Source DB: PubMed Journal: J Clin Neurophysiol ISSN: 0736-0258 Impact factor: 2.177