Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Genetic linkage, genome mismatch scanning, and analysis of patients with alterations of chromosome 6 have indicated that a major locus for development of the anterior segment of the eye, IRID1, is located at 6p25. Abnormalities of this locus lead to glaucoma. FKHL7 (also called "FREAC3"),...

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Bibliografski detalji
Glavni autori: Mears, A J, Jordan, T, Mirzayans, F, Dubois, S, Kume, T, Parlee, M, Ritch, R, Koop, B, Kuo, W L, Collins, C, Marshall, J, Gould, D B, Pearce, W, Carlsson, P, Enerbäck, S, Morissette, J, Bhattacharya, S, Hogan, B, Raymond, V, Walter, M A
Format: Artigo
Jezik:Inglês
Izdano: 1998
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377542/
https://ncbi.nlm.nih.gov/pubmed/9792859
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