Evidence of genetic heterogeneity in Alberta Hutterites with Usher syndrome type I

PURPOSE: To identify the genetic defect in a Hutterite population from northern Alberta with Usher syndrome type I. METHODS: Complete ophthalmic examinations were conducted on two boys and two girls from two related Hutterite families diagnosed with Usher syndrome type I. DNA from patients and their...

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Detalles Bibliográficos
Autores principales: Zhou, Qi, Lenger, Chaeli, Smith, Richard, Kimberling, William J, Ye, Ming, Lehmann, Ordan, MacDonald, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369897/
https://www.ncbi.nlm.nih.gov/pubmed/22690115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3369897/
https://www.ncbi.nlm.nih.gov/pubmed/22690115

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