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Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders. (2017)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddx261

PubMed Identifier: 28977442

Publication URI: http://europepmc.org/abstract/MED/28977442

Type: Journal Article/Review

Volume: 26

Parent Publication: Human molecular genetics

Issue: R2

ISSN: 0964-6906