Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3
Publication year
1995Source
Human Molecular Genetics, 4, 8, (1995), pp. 1467-1469ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Journal title
Human Molecular Genetics
Volume
vol. 4
Issue
iss. 8
Page start
p. 1467
Page end
p. 1469
This item appears in the following Collection(s)
- Academic publications [204980]
- Electronic publications [103240]
- Faculty of Medical Sciences [81051]
- Open Access publications [71779]
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