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Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients

✍ Scribed by Marie Wattenhofer; Mario Di Iorio; Raquel Rabionet; Loretta Dougherty; Andreas Pampanos; Torsten Schwede; Barbara Montserrat-Sentis; Maria Arbones; Theofilos Iliades; Annamaria Pasquadibisceglie; Marcello D'Amelio; Sura Alwan; Colette Rossier; Hans-Henrik M. Dahl; Michael B. Petersen; Xavier Estivill; Paolo Gasparini; Hamish S. Scott; Stylianos E. Antonarakis

Publisher: Springer
Year: 2002
Tongue: English
Weight: 169 KB
Volume: 80
Category: Article
ISSN: 0946-2716
DOI: 10.1007/s00109-001-0310-6

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