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

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Publication year
1995
Author(s)
Bitner-Glindzicz, M.
Turnpenny, P.
Höglund, P.
Kääriäinen, H.
Sankila, E.M.
Maarel, S.M. van der
Kok, Y.J.M. de
Ropers, H.-H.
Cremers, F.P.M.
Pembrey, M.
Malcolm, S.
Source
Human Molecular Genetics, 4, 8, (1995), pp. 1467-1469
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/22078   https://hdl.handle.net/2066/22078
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