The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology and Child Health
Reference30 articles.
1. Homeobox Genes in the Developing Mouse Brain
2. 1 Homeobox Gene Expression during Development of the Vertebrate Brain
3. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
4. Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
5. HESX1: a novel gene implicated in a familial form of septo-optic dysplasia
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