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Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts
PURPOSE: To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in a consanguineous family. METHODS: All family members participating in the study received a comprehensive ophthalmic examination to determine their ocular phenotype and contributed a blood sam...
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Publicado no: | PLoS One |
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Main Authors: | , , , , , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Public Library of Science
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5096708/ https://ncbi.nlm.nih.gov/pubmed/27814360 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0162620 |
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