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A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder. (2021)

First Author: Ammous Z

Attributed to: Precision Medicine Exeter Innovation Platform (PMEI Platform) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1371/journal.pgen.1009803

PubMed Identifier: 34570759

Publication URI: http://europepmc.org/abstract/MED/34570759

Type: Journal Article/Review

Volume: 17

Parent Publication: PLoS genetics

Issue: 9

ISSN: 1553-7390