RecName: Full=Usherin; AltName: Full=Usher syndrome type IIa protein h - Protein

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Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing. [Orphanet J Rare Dis. 2013]
Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.
Yang T, Wei X, Chai Y, Li L, Wu H. Orphanet J Rare Dis. 2013 Jun 14; 8:85. Epub 2013 Jun 14.
Usher syndrome type 2 caused by activation of an USH2A pseudoexon: implications for diagnosis and therapy. [Hum Mutat. 2012]
Usher syndrome type 2 caused by activation of an USH2A pseudoexon: implications for diagnosis and therapy.
Vaché C, Besnard T, le Berre P, García-García G, Baux D, Larrieu L, Abadie C, Blanchet C, Bolz HJ, Millan J, et al. Hum Mutat. 2012 Jan; 33(1):104-8. Epub 2011 Nov 16.
Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa. [J Med Genet. 2010]
Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.
McGee TL, Seyedahmadi BJ, Sweeney MO, Dryja TP, Berson EL. J Med Genet. 2010 Jul; 47(7):499-506. Epub 2010 May 27.

RefSeq protein
See the reference protein sequence for usherin precursor (NP_001289148.1).

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RecName: Full=Usherin; AltName: Full=Usher syndrome type IIa protein homolog; Al...
RecName: Full=Usherin; AltName: Full=Usher syndrome type IIa protein homolog; AltName: Full=Usher syndrome type-2A protein homolog; Flags: Precursor
gi|1531253870|sp|Q8K3K1.2|USH2A_RAT

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