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Updated: May 5, 2026

06:41
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome
C Lacoste1, B Leheup, I Agouti
1Assistance Publique-Hôpitaux de Marseille, Laboratoire de Génétique Moléculaire, Hôpital d'enfants de la Timone, Marseille, France; UMR_S 910 INSERM-AMU, Marseille, France.
Clinical Genetics
|December 3, 2013
Abstract
No abstract available in PubMed .
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