A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25

Genomics

Volumn 63, Issue 1, 2000, Pages 1-6

  Morell, Robert J ^a   Friderici, Karen H ^b   Wei, Sainan ^c   Elfenbein, Jill L ^d   Friedman, Thomas B ^a   Fisher, Rachel A ^c  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b Michigan State University ^*  (United States)

^c MICHIGAN STATE UNIVERSITY   (United States)

^d MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGE; ARTICLE; CHROMOSOME 17Q; FAMILY; GENE LOCATION; GENE LOCUS; GENETIC LINKAGE; GENOME; HAPLOTYPE; HEARING LOSS; HUMAN; PATHOGENESIS; PERCEPTION DEAFNESS; PRIORITY JOURNAL;

EID: 0034002166     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1999.6058     Document Type: Article

References (26)

1. Deloukas P., Schuler G. D., Gyapay G., Beasley E. M., Soderlund C. A physical map of 30,000 human genes. Science. 282:1998;744-746.
2. Drabkin H., Kao F. T., Hartz J., Hart I., Gazdar A. Localization of human ERBA2 to the 3p22-3p24.1 region of chromosome 3 and variable deletion in small cell lung cancer. Proc. Natl. Acad. Sci. USA. 85:1988;9258-9262.
3. Forrest D., Erway L. C., Ng L., Altschuler R., Curran T. Thyroid hormone receptor beta is essential for development of auditory function. Nat. Genet. 13:1996a;354-357.
4. Forrest D., Golarai G., Connor J., Curran T. Genetic analysis of thyroid hormone receptors in development and disease. Rec. Prog. Horm. Res. 51:1996b;1-22.
5. Forrest D., Hanebuth E., Smeyne R. J., Everds N., Stewart C. L. Recessive resistance to thyroid hormone in mice lacking thyroid hormone receptor beta: Evidence for tissue-specific modulation of receptor function. EMBO J. 15:1996c;3006-3015.
6. Foster J. W., Schafer A. J., Critcher R., Spillett D. J., Feakes R. W. A high-resolution whole genome radiation hybrid map of human chromosome 17q22-q25.3 across the genes for GH and TK. Genomics. 33:1996;185-192.
7. Gosden J. R., Middleton P. G., Rout D., De Angelis C. Chromosomal localization of the human oncogene ERBA2. Cytogenet. Cell. Genet. 43:1986;150-153.
8. Hampton, L. L, Morell, R. J, Morton, C. C, and, Battey, J. F. 1999, Identification of novel sequences expressed in the human fetal cochlea. Association for Research in Otolaryngology, Midwinter Research Meeting. [Abstract 37].
9. Hulander M., Wurst W., Carlsson P., Enerbäck S. The winged helix transcription factor Fkh10 is required for normal development of the inner ear. Nat. Genet. 20:1998;374-376.
10. International RH Mapping Consortium and National Center for Biotechnology Information, 1999, A new gene map of the human genome, National Library of Medicine, Bethesda, MD. Available at, http://www.ncbi.nlm.nih.gov/genemap/ .
11. Lathrop G. M., Lalouel J. M. Easy calculations of lod scores and genetic risks on small computers. Am. J. Hum. Genet. 36:1984;460-465.
12. Le Beau M. M., Espinosa R. D., Neuman W. L., Stock W., Roulston D. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases. Proc. Natl. Acad. Sci. USA. 90:1993;5484-5488.
13. Lunetta K., Boehnke M., Lange K., Cox D. R. Selected locus and multiple panel models for radiation hybrid mapping. Am. J. Hum. Genet. 59:1996;717-725.
14. Meulenbelt I., Droog S., Trommelen G. J. M., Boomsma D. I., Slagboom P. E. High-yield noninvasive human genomic DNA isolation method for genetic studies in geographically dispersed families and populations. Am. J. Hum. Genet. 57:1995;1252-1254.
15. Morton N. E. Genetic epidemiology of hearing impairment. Ann. N. Y. Acad. Sci. 630:1991;16-31.
16. Murphy D. B., Seemann S., Wiese S., Kirschner R., Grzeschik K. H. The human hepatocyte nuclear factor 3/fork head gene FKHL13: Genomic structure and pattern of expression. Genomics. 40:1997;462-469.
17. Popescu N. C., Cheng S. Y., Pastan I. Chromosomal localization of the gene for a human thyroid hormone-binding protein. Am. J. Hum. Genet. 42:1988;560-564.
18. Rusch A., Erway L. C., Oliver D., Vennstrom B., Forrest D. Thyroid hormone receptor beta-dependent expression of a potassium conductance in inner hair cells at the onset of hearing. Proc. Natl. Acad. Sci. USA. 95:1998;15758-15762.
19. Schäffer A. A. Faster linkage analysis computations for pedigrees with loops or unused alleles. Hum. Hered. 46:1996;226-235.
20. Schuler G. D., Boguski M. S., Stewart E. A., Stein L. D., Gyapay G. A gene map of the human genome. Science. 274:1996;540-546.
21. Skvorak A. B., Weng Z., Yee A. J., Robertson N. G., Morton C. C. Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness. Hum. Mol. Genet. 8:1999;439-452.
22. Solovyev V. V., Salamov A. A. The Gene-Finder computer tools for analysis of human and model organisms genome sequences. Rawling C., Clark D., Altman R., Hunter L., Lengauer T. Fifth International Conference on Intelligent Systems for Molecular Biology. 1997;294-302 AAAI Press, Halkidiki.
23. Terwilliger J. D., Ott J. Handbook of Human Genetic Linkage. 1994;Johns Hopkins Univ. Press, Baltimore.
24. Ueyama H., Inazawa J., Nishino H., Ohkubo I., Miwa T. FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenes. Cytogenet. Cell Genet. 74:1996;221-224.
25. Van Camp, G, and, Smith, R. 1999, Hereditary hearing loss homepage. World Wide Web URL, http://dnalab-www.uia.ac.be/dnalab/hhh/ .
26. Wagner T., Tommerup N., Wirth J., Leffers H., Zimmer J. A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3. Cytogenet. Cell. Genet. 76:1997;172-175.