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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Ponnam, Surya Prakash G., Ramesha, Kekunnaya, Tejwani, Sushma, Matalia, Jyoti, Kannabiran, Chitra
Format: Artigo
Sprache:Inglês
Veröffentlicht: Molecular Vision 2008
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2442473/
https://ncbi.nlm.nih.gov/pubmed/18596884
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge