Mapping of a congenital microcoria locus to 13q31-q32.

Congenital microcoria is an autosomal dominant disorder characterized by a pupil with a diameter <2 mm. It is thought to be due to a maldevelopment of the dilator pupillae muscle of the iris, and it is associated with juvenile-onset glaucoma. A total genome search for the location of the congenit...

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Bibliografiska uppgifter
Huvudupphovsmän: Rouillac, C, Roche, O, Marchant, D, Bachner, L, Kobetz, A, Toulemont, P J, Orssaud, C, Urvoy, M, Odent, S, Le Marec, B, Abitbol, M, Dufier, J L
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1998
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377098/
https://ncbi.nlm.nih.gov/pubmed/9545411
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