-
1
-
-
0030960855
-
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
-
(1997)
Nat. Genet.
, vol.16
, pp. 188-190
-
-
Liu, X.Z.1
-
2
-
-
0030951102
-
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
-
(1997)
Nat. Genet.
, vol.16
, pp. 191-193
-
-
Weil, D.1
-
3
-
-
17644442703
-
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene
-
(1998)
Science
, vol.280
, pp. 1444-1447
-
-
Probst, F.J.1
-
4
-
-
0031007349
-
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
-
(1997)
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
-
5
-
-
17344373747
-
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
-
(1998)
Nat. Genet.
, vol.20
, pp. 370-373
-
-
Xia, J.H.1
-
6
-
-
0028988233
-
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
-
(1995)
Science
, vol.267
, pp. 685-688
-
-
De Kok, Y.J.1
-
7
-
-
7144257859
-
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans
-
(1998)
Science
, vol.279
, pp. 1950-1954
-
-
Vahava, O.1
-
8
-
-
17344364928
-
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
-
(1998)
Nat. Genet.
, vol.19
, pp. 60-62
-
-
Verhoeven, K.1
-
9
-
-
0032977996
-
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 409-412
-
-
Mustapha, M.1
-
10
-
-
17344363707
-
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
-
(1998)
Nat. Genet.
, vol.20
, pp. 299-303
-
-
Robertson, N.G.1
-
11
-
-
0032011145
-
A mutation in PDS causes non-syndromic recessive deafness
-
(1998)
Nat. Genet.
, vol.18
, pp. 215-217
-
-
Li, X.C.1
-
12
-
-
0027226069
-
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
-
(1993)
Nat. Genet.
, vol.4
, pp. 289-294
-
-
Prezant, T.R.1
-
13
-
-
0028815440
-
Defective myosin VIIA gene responsible for Usher syndrome type 1B
-
(1995)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
-
15
-
-
0028860302
-
A type VII myosin encoded by the mouse deafness gene shaker-1
-
(1995)
Nature
, vol.374
, pp. 62-64
-
-
Gibson, F.1
-
16
-
-
7944229728
-
Retinitis pigmentosa combined with congenital deafness; with vestibulo-cerebellar ataxia and mental abnormality in a proportion of cases: A clinical and genetic statistic study
-
(1959)
Acta Psychiatr. Scand.
, vol.34
, pp. 5-101
-
-
Hallgren, B.1
-
22
-
-
0000870234
-
The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse
-
(1956)
Proc. R. Soc. Lond. B
, vol.145
, pp. 206-213
-
-
Deol, M.S.1
-
24
-
-
0030973305
-
Unconventional myosins in inner-ear sensory epithelia
-
(1997)
J. Cell Biol.
, vol.137
, pp. 1287-1307
-
-
Hasson, T.1
-
26
-
-
0031865677
-
Oculomotor testing in the differential diagnosis of degenerative ataxic disorders
-
(1998)
Arch. Neurol.
, vol.55
, pp. 949-956
-
-
Wessel, K.1
-
27
-
-
0028256473
-
Oculomotor abnormalities and MRI findings in idiopathic cerebellar ataxia
-
(1994)
J. Neurol.
, vol.241
, pp. 234-241
-
-
Fetter, M.1
-
28
-
-
0031151943
-
Gain adaptation and phase dynamics of compensatory eye movements in mice
-
(1997)
Genes Funct.
, vol.1
, pp. 175-190
-
-
Koekkoek, S.K.1
-
29
-
-
0028784445
-
Phase relations of Purkinje cells in the rabbit flocculus during compensatory eye movements
-
(1995)
J. Neurophysiol.
, vol.74
, pp. 2051-2064
-
-
De Zeeuw, C.I.1
-
30
-
-
0030057741
-
Pattern of selected calcium-binding proteins in the vestibular nuclear complex of two rodent species
-
(1996)
J. Comp. Neurol.
, vol.365
, pp. 575-584
-
-
Kevetter, G.A.1
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