Journal article
Gene Mapping Of The Usher Syndromes
Otolaryngologic clinics of North America, Vol.25(5), pp.923-934
10/1992
DOI: 10.1016/S0030-6665(20)30915-4
PMID: 1408196
Abstract
The successful search for the Usher genes is complicated by the factors of diagnosis and genetic heterogeneity. At least four different genetic types of Usher syndrome are believed to exist. Two types have been localized: one type II to human chromosome lq and type I to chromosome 14. As more Usher genes are localized, identified, and then sequenced, a better understanding of the nature of the clinical variation of Usher syndrome will be gained.
Details
- Title: Subtitle
- Gene Mapping Of The Usher Syndromes
- Creators
- William KimberlingRichard J.H Smith
- Resource Type
- Journal article
- Publication Details
- Otolaryngologic clinics of North America, Vol.25(5), pp.923-934
- DOI
- 10.1016/S0030-6665(20)30915-4
- PMID
- 1408196
- NLM abbreviation
- Otolaryngol Clin North Am
- ISSN
- 0030-6665
- eISSN
- 1557-8259
- Language
- English
- Date published
- 10/1992
- 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
- 9984006321502771
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