ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm
Published inHuman Molecular Genetics, vol. 22, no. 16, p. 3250-3258
Publication date2013
Abstract
Keywords
- MATTHEW-WOOD-SYNDROME
- RETINOIC ACID
- STRA6 MUTATIONS
- ANOPHTHALMIA
- EYE
- COLOBOMA
- SPECTRUM
- RECEPTOR
- MICROPHTHALMIA
- DEFECTS
Affiliation Not a UNIGE publication
Research group
Citation (ISO format)
YAHYAVI, Mani et al. ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm. In: Human Molecular Genetics, 2013, vol. 22, n° 16, p. 3250–3258. doi: 10.1093/hmg/ddt179
Main files (1)
Article (Published version)
![accessLevelRestricted](assets/images/access-level-restricted.png)
Identifiers
- PID : unige:142250
- DOI : 10.1093/hmg/ddt179
- PMID : 23591992
ISSN of the journal0964-6906