A missense mutation in LIM2 causes autosomal recessive congenital cataract

PURPOSE: To identify mutations in the LIM2 gene in families with hereditary congenital or juvenile-onset cataract. METHODS: Forty families (total of 100 affected and 84 unaffected individuals) were recruited for the study. Probands were screened for pathogenic alterations in 10 different candidate g...

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Detalles Bibliográficos
Autores principales: Ponnam, Surya Prakash G., Ramesha, Kekunnaya, Tejwani, Sushma, Matalia, Jyoti, Kannabiran, Chitra
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2008
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442473/
https://www.ncbi.nlm.nih.gov/pubmed/18596884

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442473/
https://www.ncbi.nlm.nih.gov/pubmed/18596884

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