Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A. (2019)

First Author: Tao F

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/ana.25426

PubMed Identifier: 30706531

Publication URI: http://europepmc.org/abstract/MED/30706531

Type: Journal Article/Review

Volume: 85

Parent Publication: Annals of neurology

Issue: 3

ISSN: 0364-5134