A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration [10]

American Journal of Human Genetics

Volumn 64, Issue 1, 1999, Pages 318-323

  Lalwani, A K ^a   Luxford, W M ^a   Mhatre, A N ^a   Attaie, A ^a   Wilcox, E R ^a   Castelein, C M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

CHROMOSOME 22; CHROMOSOME MAP; CLINICAL ARTICLE; FAMILY STUDY; GENE ISOLATION; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; HAPLOTYPE; HEARING IMPAIRMENT; HISTOPATHOLOGY; HUMAN; INNER EAR DISEASE; LETTER; PATHOGENESIS; PRIORITY JOURNAL;

EID: 0033364309     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302216     Document Type: Letter

References (29)

1. KS Arnos J Israel L Devlin MP Wilson Genetic counseling for the deaf Otolaryngol Clin North Am 25 1992 953 971
2. L Bergstrom Pathology of congenital deafness: present status and future priorities Ann Otol Rhinol Laryngol Suppl 89 1980 31 42
3. GR Bock KP Steel Inner ear pathology in the deafness mutant mouse Acta Otolaryngol (Stockh) 96 1983 39 47
4. M Boehnke Estimating the power of a proposed linkage study: a practical computer simulation approach Am J Hum Genet 39 1986 513 527
5. PJ Brookhouser Hereditary hearing loss GA Gates Current therapy in otolaryngology—head and neck surgery 5th ed 1994 Mosby St. Louis 44 52
6. MM Cohen RJ Gorlin Epidemiology, etiology and genetic patterns RJ Gorlin HV Toriello MM Cohen Hereditary hearing loss and its syndromes 1995 Oxford University Press New York 9 21
7. RW Cottingham Jr RM Idury AA Schäffer Faster sequential genetic linkage computations Am J Hum Genet 53 1993 252 263
8. F Denoyelle G Lina-Granade H Plauchu R Bruzzone H Chaib F Levi-Acobas D Weil Connexin 26 gene linked to a dominant deafness Nature 393 1998 319 320
9. GR Fraser The causes of profound deafness in childhood: a study of 3,535 individuals with severe hearing loss present at birth or of childhood onset 1995 Johns Hopkins University Press Baltimore
10. AJ Gulya NR Juhlin Histopathology of deafness Ear Nose Throat J 71 1992 494 499-502
11. U Khetarpal Autosomal dominant sensorineural hearing loss: further temporal bone findings Arch Otolaryngol Head Neck Surg 119 1993 106 108
12. U Khetarpal HF Schuknecht RR Gacek LB Holmes Autosomal dominant sensorineural hearing loss: pedigrees, audiologic findings, and temporal bone findings in two kindreds Arch Otolaryngol Head Neck Surg 117 1991 1032 1042
13. AK Lalwani CM Castelein Inherited hearing loss: cracking the auditory genetic code, part I: nonsyndromic Am J Otol 20 1999 115 132
14. AK Lalwani FH Linthicum ER Wilcox JK Moore FC Walters TB San Agustin J Mislinski A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration Audiol Neurootol 2 1997 139 154
15. XZ Liu J Walsh Y Tamagawa K Kitamura M Nishizawa KP Steel SD Brown Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene Nat Genet 17 1997 268 269
16. ED Lynch MK Lee JE Morrow PL Welsch PE Leaon MC King Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous Science 278 1997 1315 1318
17. IW Mair Hereditary deafness in the white cat Acta Otolaryngol Suppl (Stockh) 314 1973 1 48
18. EN Manolis N Yandavi JB Nadol Jr RD Eavey M McKenna S Rosenbaum U Khetarpal A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13 Hum Mol Genet 5 1996 1047 1050
19. FC Ormerod The pathology of congenital deafness J Laryngol Otol 74 1960 919 950
20. PW Reed JL Davies JB Copeman ST Bennett SM Palmer LE Pritchard SC Gough Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping Nat Genet 7 1994 390 395
21. CG Saez JC Myers TB Shows LA Leinwand Human nonmuscle myosin heavy chain mRNA: generation of diversity through alternative polyadenylylation Proc Natl Acad Sci USA 87 1990 1164 1168
22. AA Schäffer SK Gupta K Shriram RW Cottingham Jr Avoiding recomputation in linkage analysis Hum Hered 44 1994 225 237
23. M Simons M Wang OW McBride S Kawamoto K Yamakawa D Gdula RS Adelstein Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes Circ Res 69 1991 530 539
24. KP Steel GR Bock Hereditary inner-ear abnormalities in animals: relationships with human abnormalities Arch Otolaryngol 109 1983 22 29
25. LE Toothaker DA Gonzalez N Tung RS Lemons MM Le Beau MA Arnaout LK Clayton Cellular myosin heavy chain in human leukocytes: isolation of 5′ cDNA clones, characterization of the protein, chromosomal localization, and upregulation during myeloid differentiation Blood 78 1991 1826 1833
26. O Vahava R Morell ED Lynch S Weiss ME Kagan N Ahituv JE Morrow Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans Science 279 1998 1950 1954
27. K Verhoeven L Van Laer K Kirschhofer PK Legan DC Hughes I Schatteman M Verstreken Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment Nat Genet 19 1998 60 62
28. A Wang Y Liang RA Fridell FJ Probst ER Wilcox JW Touchman CC Morton Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3 Science 280 1998 1447 1451
29. JL Weber PE May Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction Am J Hum Genet 44 1989 388 396