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A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV). (2017)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.23123

PubMed Identifier: 27676246

Publication URI: http://europepmc.org/abstract/MED/27676246

Type: Journal Article/Review

Volume: 38

Parent Publication: Human mutation

Issue: 1

ISSN: 1059-7794