Analysis of intragenic USH2A copy number variation unveils broad spectrum of unique and recurrent variants

Author:

Austin-Tse Christina A.,Mandelker Diana L.,Oza Andrea M.,Mason-Suares Heather,Rehm Heidi L.,Amr Sami S.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference39 articles.

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5. Molecular and in silico analyses of the full-length isoform of usherin identify new pathogenic alleles in Usher type II patients;Baux;Hum. Mutat.,2007

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