SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvement. (2017)

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s10048-016-0505-1

PubMed Identifier: 28005197

Publication URI: http://europepmc.org/abstract/MED/28005197

Type: Journal Article/Review

Volume: 18

Parent Publication: Neurogenetics

Issue: 1

ISSN: 1364-6745