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The genetics of aniridia — simple things become complicated
Aniridia is a rare, panocular disorder characterized by a variable degree of hypoplasia or the absence of iris tissue associated with additional ocular abnormalities. It is inherited in an autosomal dominant manner, with high penetrance and variable expression even within the same family. In most ca...
Gardado en:
| Publicado en: | J Appl Genet |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer Berlin Heidelberg
2018
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5895662/ https://ncbi.nlm.nih.gov/pubmed/29460221 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13353-017-0426-1 |
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