📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

Deep geno- and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutation. (2021)

First Author: Khani M
Attributed to:  Understanding the genes for Parkinson's disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00415-020-10171-4

PubMed Identifier: 32897397

Publication URI: http://europepmc.org/abstract/MED/32897397

Type: Journal Article/Review

Volume: 268

Parent Publication: Journal of neurology

Issue: 2

ISSN: 0340-5354