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  4. Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
 
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Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss

Journal
HUMAN MOLECULAR GENETICS
ISSN
0964-6906
Author(s)
Bassani Sissy
Van Beelen Edward
Rossel Mireille
Voisin Norine
Morgan Anna 
Arribat Yoan
Chatron Nicolas
Chrast Jacqueline
Cocca Massimiliano 
Delprat Benjamin
Faletra Flavio 
Giannuzzi Giuliana
Guex Nicolas
Machavoine Roxane
Pradervand Sylvain
Smits Jeroen J.
Van De Kamp Jiddeke M.
Ziegler Alban
Amati Francesca
Marlin Sandrine
Kremer Hannie
Locher Heiko
Maurice Tangui
Gasparini Paolo 
Girotto Giorgia 
Reymond Alexandre
DOI
10.1093/hmg/ddab145
Project(s)
Identification of new genes/variants involved in hearing function and loss 
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C.A.R.S.O. - I.R.C.C.S. materno infantile Burlo Garofolo

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