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Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss

✍ Scribed by Freitas, Érika L.; Oiticica, Jeanne; Silva, Amanda G.; Bittar, Roseli S.M.; Rosenberg, Carla; Mingroni-Netto, Regina C.


Book ID
125433409
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
924 KB
Volume
57
Category
Article
ISSN
1769-7212

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