Current understanding of usher syndrome type II

Usher syndrome is the most common deafness-blindness caused by genetic mutations. To date, three genes have been identified underlying the most prevalent form of Usher syndrome, the type II form (USH2). The proteins encoded by these genes are demonstrated to form a complex in vivo. This complex is l...

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Veröffentlicht in:	Frontiers in bioscience 2012-01, Vol.17 (3), p.1165-1183
Hauptverfasser:	Yang, Jun, Wang, Le, Song, Hongman, Sokolov, Maxim
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Disease Models, Animal Extracellular Matrix Proteins - metabolism Humans Mice Usher Syndromes - genetics Usher Syndromes - metabolism Usher Syndromes - physiopathology
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