DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Nonsyndromic Autosomal Dominant Hearing Loss Journal Articles Refereed uri icon

Overview

Authors

  • Authorship

    • A/PROF Michael Hildebrand
    • WORKMAN H
    • DELUCA AP
    • DEL CASTILLO I
    • TAYLOR KR
    • TOMPKINS B
    • GOODMAN CW
    • SCHRAUWEN I
    • VAN WESEMAEL M
    • LACHLAN K
    • SHEARER AE
    • MORIN M
    • BRAUN TA
    • HUYGEN PLM
    • KREMER H
    • VAN CAMP G
    • MORENO F
    • CASAVANT TL
    • SMITH RJH
    • MORENO-PELAYO MA
    • MEYER NC
    • MAYO F
    • MODAMIO-HOYBJOR S
    • MENCIA A
    • OLAVARRIETA L
    • MORALES-ANGULO C
    • NISHIMURA CJ

Published in

  • Human Mutation

Time

Date/time value

  • 2011

Identity

Digital Object Identifier (DOI)

  • 10.1002/humu.21512

Additional Document Info

Parent Title

  • HUMAN MUTATION

Volume

  • 32

Issue

  • 7

Publisher

  • Wiley-Liss