Concepedia

Publication | Closed Access

Further mutations in <i>Brain 4</i> (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

DOI

84

Citations

0

References

1995

Year

Maria Bitner‐Glindzicz, Peter D. Turnpenny, Pia Höglund, Helena Kääriäinen, Eeva‐Marja Sankila, Silvère M. van der Maarel, Yvette J.M. de Kok, Hans‐Hilger Ropers, Frans P.M. Cremers, Marcus Pembrey,
Human Molecular Genetics

Abstract

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