A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation.
Publication year
2001Source
Journal of Medical Genetics, 38, 1, (2001), pp. 61-5ISSN
Publication type
Article / Letter to editor
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Organization
Otorhinolaryngology
Human Genetics
Journal title
Journal of Medical Genetics
Volume
vol. 38
Issue
iss. 1
Page start
p. 61
Page end
p. 5
Subject
Hereditary and acquired vitreo-retinal disorders: experimental and clinical research and treatment.; Hearing and Communication Disorders; Erfelijke en verworven vitreo-retinale aandoeningen: experimenteel en klinisch onderzoek en behandeling.; Gehoor en communicatieThis item appears in the following Collection(s)
- Academic publications [245410]
- Faculty of Medical Sciences [93205]
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