Open AccessThe molecular basis of X‐linked deafness type 3 (DFN3) in two sporadic cases: Identification of a somatic mosaicism for a POU3F4 missense mutation
Author(s) -
Y.J.M. de Kok,
C.W.R.J. Cremers,
HansHilger Ropers,
Frans P.M. Cremers
Publication year - 1997
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1997)10:3<207::aid-humu5>3.3.co;2-x
Subject(s) - missense mutation , biology , pou domain , genetics , mutation , point mutation , somatic cell , homeobox , microbiology and biotechnology , gene , transcription factor