Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues**Nucleotide sequence data reported herein are available in the DDBJ/EMBL/GenBank databases; for details, see the Electronic-Database Information section of this article.
- 1 January 2003
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 72 (1) , 73-82
- https://doi.org/10.1086/345398
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Genome-Wide Profiling of Gene Expression in 29 Normal Human Tissues with a cDNA MicroarrayDNA Research, 2002
- Targeted disruption of Otog results in deafness and severe imbalanceNature Genetics, 2000
- Prevalent connexin 26 gene (GJB2) mutations in JapaneseJournal of Medical Genetics, 2000
- Prevalence of mitochondrial gene mutations among hearing impaired patientsJournal of Medical Genetics, 2000
- Identification of the stef Gene That Encodes a Novel Guanine Nucleotide Exchange Factor Specific for Rac1Journal of Biological Chemistry, 1999
- The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequencyHearing Research, 1996
- Responsiveness of α1, and β1Cochlear Na, K-ATPase Isoforms to Thyroid HormoneActa Oto-Laryngologica, 1996
- Isolation of Novel and Known Genes from a Human Fetal Cochlear cDNA Library Using Subtractive Hybridization and Differential ScreeningGenomics, 1994
- Genetic epidemiological studies of early‐onset deafness in the U.S. school‐age populationAmerican Journal of Medical Genetics, 1993
- Periods of Sensitivity to Thyroid Hormone during the Development of the Organ of CortiActa Oto-Laryngologica, 1986