New gene for automosol recessive non-syndromic hearing loss maps to either chromosome 3q or 19p

American Journal of Medical Genetics

Volumn 71, Issue 4, 1997, Pages 467-471

  Chen, Achih ^a   Wayne, Sigrid ^a   Bell, Adam ^a   Ramesh, Arabandi ^b   Srisailapathy, C R Srikumari ^b   Scott, Daryl A ^c   Sheffield, Val C ^c   Van Hauwe, Peter ^d   Zbar, Ross I S ^a   Ashley, Jennifer ^e   Lovett, Michael ^e   Van Camp, Guy ^d   Smith, Richard J H ^a  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF MADRAS   (India)

^c UNIVERSITY OF IOWA   (United States)

^d UNIVERSITY OF ANTWERP   (Belgium)

^e UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

Autosomal recessive non syndromic hearing impairement; Homozygosity mapping

Indexed keywords

ARTICLE; AUDIOMETRY; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 19P; CHROMOSOME 3Q; DRUG USE; GENE LOCUS; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENOME; HEARING IMPAIRMENT; HEARING LOSS; HOMOZYGOSITY; HUMAN; MENINGITIS; PERINATAL CARE; PREMATURITY; PRIORITY JOURNAL; RUBELLA;

ALGORITHMS; AUDIOMETRY; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 3; DNA; FEMALE; GENE FREQUENCY; GENES, RECESSIVE; GENETIC MARKERS; GENOME, HUMAN; GENOMIC IMPRINTING; HEARING LOSS; HUMANS; LOD SCORE; MALE; NUCLEAR FAMILY; PEDIGREE; POLYMORPHISM, GENETIC; PREGNANCY;

EID: 0030796428     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: None     Document Type: Article

References (37)

1. Ben Arab S, Bonaïti-Pellié C, Belkahia A (1990): An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul). J Med Genet 27:29-33.
2. Bergstrom L, Hemenway WG, Down MP (1971): A high risk registry to find congenital deafness. Otolaryngol Clin North Am 4:369-399.
3. Chaib H, Place C, Salem N, Dode C, Chardenoux S, Weissenbach J, El-Zir E, Loiselet J, Petit C (1996): Mapping of DFNB12, a gene for non-syndromal autosomal recessive deafness, to chromosome 10q21-22. Hum Mol Genet 5:1061-1064.
4. Chung CS, Brown KS (1970): Family studies of early childhood deafness ascertained through the Clarke School for the Deaf. Am J Hum Genet 22:630-644.
5. Chung CS, Robison OW, Morton NE (1959): A note on deaf mutism. Ann Hum Genet 23:357-366.
6. Deol MS, Robins MW (1962): The spinner mouse. J Hered 53:133-136.
7. Fraser GR (1976): "The Causes of Profound Deafness in Childhood." Johns Hopkins Baltimore: University Press.
8. Froidevaux S, Loor F (1991): A quick procedure for identifying doubly homozygous immunodeficient scid beige mice. J Immunol Meth 137: 275-279.
9. Goodyear R, Holley M, Richardson G (1994): Hair and supporting-cell differentiation during the development of the avian inner ear. J Comp Neurol 351:81-93.
10. Grimberg J, Nawoschik S, Belluscio L, McKee R, Turck A, Eisenber A (1989): A simple and efficient non-organic procedure for the isolation of genomic DNA from blood. Nucleic Acids Res 17:390.
11. Gu Y, Hukriede NA, Fleming RJ (1995): Serrate expression can function-ally replace Delta activity during neuroblast segregation in the Drosophila embryo. Development 121:855-885.
12. Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C (1994): A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum Mol Genet 3:989-993.
13. Hasson T, Skowron JF, Gilbert DJ, Avraham KB, Perry WL, Bement WM, Anderson BL, Sherr EH, Chen Z-Y, Greene LA, Ward DC, Corey DP, Mooseker MS, Copeland NG, Jenkins NA (1996): Mapping of unconventional myosins in mouse and humans. Genomics 36:431-439.
14. Heitzler P, Simpson P (1991): The choice of cell fate in the epidermis of Drosophila. Cell 64:1083-1092.
15. Helwig U, Imai K, Schmahl W, Thomas BE, Varnum DS, Nadeau JH, Balling R (1995): Interaction between undulated and Patch leads to an extreme form of spina bifida in doubly-mutant mice. Nat Genet 11:60-63.
16. Kajiwara K, Berson EL, Dryja TP (1994): Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci. Science 264:1604-1608.
17. Kimberling WJ, Möller CG, Davenport S, Priluck IA, Beighton PH, Breenberg J, Reardon W, Weston MD, Kenyon JB, Grunkemeyer JA, Pieke Dahl S, Overbeck LD, Blackwood DJ, Brower AM, Hoover DM, Rowland P, Smith RJH (1992): Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11. Genomics 14:988-994.
18. Kimberling WJ, Smith SD, Ing PS, Tinley S (1989): A comment on the analysis of families with prelingual deafness. Am J Hum Genet 45: 157-158.
19. Kruglyak L, Daly M, Lander E (1995): Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping. Am J Hum Genet 56:519-527.
20. Lander E, Botstein D (1987): Homozygosity mapping: A way to map human recessive traits with the DNA of inbred children. Science 236:1567-1570.
21. Lane PW (1972): Two new mutations in linkage group XVI of the house mouse: Flaky tail and varitint-waddler-J. J Hered 63:135-140.
22. Lane PW (1987): New mutants and linkages: Deafwaddler (dfw). Mouse News Lett 77:129.
23. Lane PW, Deol MS (1974): Mocha, a new coat color and behavior mutation on chromosome 10 of the mouse. J Hered 65:362-364.
24. Lowell CA, Soriano P, Varmus HE (1994): Functional overlap in the src family: Inactivation of hck and fgr impairs natural immunity. Genes Dev 8:387-398.
25. Majumder PP, Ramesh A, Chinnappan D (1989): On the genetics of prelingual deafness. Am J Hum Genet 44:86-99.
26. McKusick VA (1992): "Mendelian Inheritance in Man," 10th edition. Johns Hopkins Baltimore: University Press.
27. Myat A, Henrique D, Ish-Horowicz D, Lewis J (1996): A chick homologue of Serrate and its relationship with Notch and Delta homologues during central neurogenesis. Dev Biol 174:233-247.
28. Prochazka M, Leiter EH, Serreze DV, Coleman DL (1987): Three recessive loci required for insulin-dependent diabetes in nonobese diabetic mice. Science 237:286-289.
29. Rolfsen RM, Erway LC (1984): Trace metals and otolith defects in mocha mice. J Hered 75:158-162.
30. Sank D (1963): Genetic aspects of early total deafness. In: Rainer JD, Altschuler KZ, Kallmann FJ (eds): "Family and Mental Health Problems in a Deaf Population." New York: Columbia University, pp 28-81.
31. Sankila E, Pakarinen L, Kääriäinen H, Aittomäki Karjalainen S, Sistonen P, de la Chapelle A (1995): Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q. Hum Mol Genet 4:93-96.
32. Sheffield VC, Weber JL, Beutow KH, Murray JC, Even DA, Wiles K, Gstier JM, Pulido JC, Yandava C, Sunden SL, Mattes G, Businga T, McClain A, Beck J, Scherpier T, Gilliam J, Zhong J, Duyk GM (1995): A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet 4:1837-1844.
33. Smith RJH, Lee EC, Kimberling WJ, Daiger SP, Pelias MZ, Keats BJB, Jay M, Bird A, Reardon W, Guest M, Ayyagari R, Hejtmancik JF (1992): Localization of two genes for Usher syndrome type I to chromosome 11. Genomics 14:995-1002.
34. Street VA, Robinson LC, Erford SK, Tempel BL (1995): Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations. Genomics 29:123-130.
35. Tamagawa Y, Kitamura K, Ishida T, Tanaka H, Tauji S, Nishizawa M (1996): A gene for a dominant form of non-syndromic sensorineural deafness (dfna11) maps within the region containing the DFNB2 recessive deafness gene. Hum Molec Genet 5:849-852.
36. Wayne S, Der Kaloustian VM, Schloss M, Polomeno R, Scott D, Hejtmancik JP, Sheffield VC, Smith RJH (1996): Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10. Hum Molec Genet (in press).
37. Well D, Blanchard S, Kaplan J, Gullford P, Gibson F, Walsh J, Mburu P, Varela A, Levillers J, Weston MD, Kelley PM, Kimberling WJ, Wagenaar M, Levi-Acobas F, Larget-Plet D, Munnich A, Steel KP, Brown SDM, Petit C (1995): Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374:60-61.