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High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases. (2022)

First Author: Hiz Kurul S

Attributed to: Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awab395

PubMed Identifier: 34791078

Publication URI: http://europepmc.org/abstract/MED/34791078

Type: Journal Article/Review

Volume: 145

Parent Publication: Brain : a journal of neurology

Issue: 4

ISSN: 0006-8950