Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3.

Authors :: Bitner-Glindzicz M
Turnpenny P
Höglund P
Kääriäinen H
Sankila EM
van der Maarel SM
de Kok YJ
Ropers HH
Cremers FP
Pembrey M
Source :: Human molecular genetics [Hum Mol Genet] 1995 Aug; Vol. 4 (8), pp. 1467-9.
Publication Year :: 1995

Subjects :: Base Sequence
DNA genetics
Female
Genetic Markers
Humans
Male
Molecular Sequence Data
POU Domain Factors
Pedigree
Phenotype
Polymorphism, Single-Stranded Conformational
Sequence Deletion
Deafness genetics
Mutation
Transcription Factors genetics
X Chromosome genetics

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