Biology Reference
In-Depth Information
domain of alpha-tectorin associated with autosomal dominant non-syndromic
hearing loss. Eur J Hum Genet 7:255-258.
Avraham, K, Hasson T, Steel K, Kingsley D, Russell L, Mooseker M, Copeland N,
Jenkins N (1995) The mouse
Snell's waltzer
deafness gene encodes an uncon-
ventional myosin required for the structural integrity of inner ear hair cells. Nat
Genet 11:369-375.
Bermingham NA, Hassan BA, Price SD, Vollrath MA, Ben-Arie N, Eatock RA,
Bellen HJ, Lysakowski A, Zoghbi HY (1999)
Math1
: An essential gene for the
generation of inner ear hair cells. Science 284:1837-1841.
Carter D, Murphy D (1999) Molecular Neuroscience. Harlow, Essex, England:
Longman.
Coucke PJ, Hauwe PV, Kelley PM, Kunst H, Schatteman I, Velzen DV, Meyers J,
Ensink RJ, Verstreken M, Declau F, Marres H, Kastury K, Bhasin S, McGuirt WT,
Smith RJ, Cremers CW, Heyning PV, Willems PJ, Smith SD, Van Camp G (1999)
Mutations in the
KCNQ4
gene are responsible for autosomal dominant deafness
in four DFNA2 families. Hum Mol Genet 8:1321-1328.
de Kok YJ, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm
S, Pembrey ME, Ropers HH, Cremers FP (1995) Association between X-linked
mixed deafness and mutations in the POU domain gene POU3F4. Science
267:685-688.
de Kok YJ, Bom SJ, Brunt TM, Kemperman MH, van Beusekom E, van der Velde-
Visser SD, Robertson NG, Morton CC, Huygen PL, Verhagen WI, Brunner HG,
Cremers CW, Cremers FP (1999) A Pro51Ser mutation in the COCH gene is asso-
ciated with late onset autosomal dominant progressive sensorineural hearing loss
with vestibular defects. Hum Mol Genet 8:361-366.
Denoyelle F, Weil D, Maw MA, Wilcox SA, Lench NJ, Allen-Powell DR, Osborn A,
Dahl HH, Middleton A, Houseman MJ, Dode C, Marlin S, Boulila-ElGaied A,
Grati M, Ayadi H, BenArab S, Bitoun P, Lina-Granade G, Godet J, Mustapha
M, Loiselet J, El-Zir E, Aubois A, Joannard A, Petit C (1997) Prelingual deafness:
High prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet
6:2173-2177.
DiLeone RJ, Russell LB, Kingsley DM (1998) An extensive 3ยข regulatory region con-
trols expression of
Bmp5
in specific anatomical structures of the mouse embryo.
Genetics 148:401-408.
Erkman L, McEvilly RJ, Luo L, Ryan AK, Hooshmand F, O'Connell SM, Keithley
EM, Rapaport DH, Ryan AF, Rosenfeld MG (1996) Role of transcription factors
Brn-3.1 and Brn-3.2 in auditory and visual system development. Nature 381:
603-606.
Estivill X, Fortina P, Surrey S, Rabionet R, Melchionda S, D'Agruma L, Mansfield
E, Rappaport E, Govea N, Mila M, Zelante L, Gasparini P (1998) Connexin-26
mutations in sporadic and inherited sensorineural deafness. Lancet 351:394-398.
Gorlin R, Toriello H, Cohen M (1995) Hereditary hearing loss and its syndromes.
New York: Oxford University Press.
Huber I, Bitner-Glindzicz M, de Kok YJ, van der Maarel SM, Ishikawa-Brush Y,
Monaco AP, Robinson D, Malcolm S, Pembrey ME, Brunner HG, Cremers FPM
(1994) X-linked mixed deafness (DFN3): Cloning and characterization of the crit-
ical region allows the identification of novel microdeletions. Hum Mol Genet
3:1151-1154.
