Mutations in the LHX2 gene are not a frequent cause of micro/anophthalmia

PURPOSE: Microphthalmia and anophthalmia are at the severe end of the spectrum of abnormalities in ocular development. A few genes (orthodenticle homeobox 2 [OTX2], retina and anterior neural fold homeobox [RAX], SRY-box 2 [SOX2], CEH10 homeodomain-containing homolog [CHX10], and growth differentiat...

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Detalles Bibliográficos
Autores principales: Desmaison, Annaïck, Vigouroux, Adeline, Rieubland, Claudine, Peres, Christine, Calvas, Patrick, Chassaing, Nicolas
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012651/
https://www.ncbi.nlm.nih.gov/pubmed/21203406

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012651/
https://www.ncbi.nlm.nih.gov/pubmed/21203406

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