Identification of three novel mutations in human EYA1 protein associated with Branchio-Oto-Renal syndrome.
Publication year
1998Source
Human Mutation, 11, (1998), pp. 443-449ISSN
Publication type
Article / Letter to editor

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Organization
Otorhinolaryngology
Journal title
Human Mutation
Volume
vol. 11
Page start
p. 443
Page end
p. 449
Subject
Genetics of hearing; Erfelijk gehoorverliesThis item appears in the following Collection(s)
- Academic publications [232014]
- Faculty of Medical Sciences [89012]
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