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The phenotypic spectrum associated with OTX2 mutations in humans. (2021)

First Author: Gregory LC

Attributed to: Human Developmental Biology Resource (HDBR): an embryonic and fetal tissue bank for functional genetics and cell-based research funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1530/eje-20-1453

PubMed Identifier: 33950863

Publication URI: http://europepmc.org/abstract/MED/33950863

Type: Journal Article/Review

Volume: 185

Parent Publication: European journal of endocrinology

Issue: 1

ISSN: 0804-4643