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Confirmation of RAX gene involvement in human anophthalmia
Microphthalmia and anophthalmia are at the severe end of the spectrum of abnormalities in ocular development. Mutations in several genes have been involved in syndromic and non-syndromic anophthalmia. Previously, RAX recessive mutations were implicated in a single patient with right anophthalmia and...
Gorde:
| Egile Nagusiak: | , , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Munksgaard
2008
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2763090/ https://ncbi.nlm.nih.gov/pubmed/18783408 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2008.01078.x |
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