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Loss-of-Function Variants in DRD1 in Infantile Parkinsonism-Dystonia. (2023)

First Author: Reid KM

Attributed to: The development of gene therapy for infantile neuroaxonal dystrophy funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3390/cells12071046

PubMed Identifier: 37048120

Publication URI: http://europepmc.org/abstract/MED/37048120

Type: Journal Article/Review

Volume: 12

Parent Publication: Cells

Issue: 7

ISSN: 2073-4409