A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

Author: Ebermann Inga   Scholl Hendrik   Charbel Issa Peter   Becirovic Elvir   Lamprecht Jürgen   Jurklies Bernhard   Millán José   Aller Elena   Mitter Diana   Bolz Hanno  

Publisher: Springer Publishing Company

ISSN: 0340-6717

Source: Human Genetics, Vol.121, Iss.2, 2007-04, pp. : 203-211

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