Aldahmesh MA, Mohammed JY, Al-Hazzaa S, Alkuraya FS. Homozygous null mutation in ODZ3 causes microphthalmia in humans. Genet Med. 2012 Jul 5. doi:10.1038/gim.2012.71. PubMed PMID: 22766609.
Relevant genes include: Ten-m (a.k.a. odz) FBgn0004449
Showing posts with label Microphthalmia. Show all posts
Showing posts with label Microphthalmia. Show all posts
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