The phenotype of DFNA13/COL11A2

Book chapter

Peer reviewed

Els M R De Leenheer, Wyman T McGuirt, Henricus P M Kunst, Patrick L M Huygen, Richard J H Smith and Cor W R J Cremers

Genetic Hearing Impairment: Its Clinical Presentations, pp.85-91

Advances in oto-rhino-laryngology, v. 61, Karger

2002

DOI: 10.1159/000066804

PMID: 12408068

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Mutation

Phenotype

Adult

Aged

Audiometry, Pure-Tone

Auditory Threshold

Child

Collagen Type XI - genetics

Hearing Loss, Sensorineural - diagnosis

Hearing Loss, Sensorineural - genetics

Humans

Middle Aged

Pedigree

Title: Subtitle: The phenotype of DFNA13/COL11A2
Creators: Els M R De Leenheer - Department of Otorhinolaryngology, University Medical Centre Nijmegen, The Netherlands
Wyman T McGuirt
Henricus P M Kunst
Patrick L M Huygen
Richard J H Smith
Cor W R J Cremers
Resource Type: Book chapter
Publication Details: Genetic Hearing Impairment: Its Clinical Presentations, pp.85-91
Publisher: Karger; New York
Series: Advances in oto-rhino-laryngology; v. 61
DOI: 10.1159/000066804
PMID: 12408068
ISSN: 0065-3071
eISSN: 1662-2847
Grant note: 5-T32-DC00040 / NIDCD NIH HHS DC03544 / NIDCD NIH HHS
Language: English
Date published: 2002
Academic Unit: Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
Record Identifier: 9984256789802771

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