The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases : identification of a somatic mosaicism for a POU3F4 missense mutation
Publication year
1997Source
Human Mutation, 10, 3, (1997), pp. 207-211ISSN
Publication type
Article / Letter to editor

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Organization
Otorhinolaryngology
Human Genetics
Journal title
Human Mutation
Volume
vol. 10
Issue
iss. 3
Page start
p. 207
Page end
p. 211
This item appears in the following Collection(s)
- Academic publications [202923]
- Electronic publications [101091]
- Faculty of Medical Sciences [80072]
- Open Access publications [69755]
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