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SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile. (2022)

First Author: Al-Jawahiri R

Attributed to: UK Infrastructure for Large-scale Clinical Genomics Research funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2022.02.013

PubMed Identifier: 35341651

Publication URI: http://europepmc.org/abstract/MED/35341651

Type: Journal Article/Review

Volume: 24

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 6

ISSN: 1098-3600