- Title
- Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
- Creators
- Richard J.H Smith - University of IowaWyman T McGuirt - University of IowaSai D Prasad - University of IowaAndrew J Griffith - National Institutes of Health, BethesdaHenricus P.M Kunst - Radboud University NijmegenGlenn E Green - University of IowaKarl B Shpargel - National Institutes of Health, BethesdaChristina Runge - University of IowaChristy Huybrechts - University of AntwerpRobert F Mueller - St James's University HospitalEric Lynch - University of WashingtonMary-Claire King - University of WashingtonHan G Brunner - Radboud University NijmegenCor W.R.J Cremers - Radboud University NijmegenMasamine Takanosu - University of Alabama at BirminghamShi-Wu Li - Drexel UniversityMachiko Arita - Drexel UniversityRichard Mayne - University of Alabama at BirminghamDarwin J Prockop - Drexel UniversityGuy Van Camp - Department of Genetics, University of AntwerpEdward F Lynch - Pathology (and Laboratory Medicine)
- Publication Details
- Nature genetics, v 23(4), pp 413-419
- Publisher
- Springer Nature
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Pathology (and Laboratory Medicine)
- Web of Science ID
- WOS:000084023900015
- Scopus ID
- 2-s2.0-0032755733
- Other Identifier
- 991019169532504721
Journal article
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
Nature genetics, v 23(4), pp 413-419
Dec 1999
PMID: 10581026
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- Collaboration types
- Domestic collaboration
- International collaboration
- Web of Science research areas
- Genetics & Heredity