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Extended mutation spectrum of Usher syndrome in Finland

✍ Scribed by Hanna Västinsalo; Reetta Jalkanen; Carsten Bergmann; Christine Neuhaus; Leenamaija Kleemola; Liisa Jauhola; Hanno Jörn Bolz; Eeva-Marja Sankila

Book ID
114925177
Publisher
Wiley (Blackwell Publishing)
Year
2012
Tongue
English
Weight
712 KB
Volume
91
Category
Article
ISSN
1755-375X

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## Communicated by Andreas Gal Usher syndrome type II (USH2) is an autosomal recessive disorder, characterised by moderate to severe high-frequency hearing impairment, normal balance function and progressive visual impairment due to retinitis pigmentosa. Usher syndrome type IIa, the most common su