|1.||Lentz, Jennifer J: 1 article (11/2011)|
|2.||Han, Philip F: 1 article (11/2011)|
|3.||Blanco-Sanchez, Bernardo: 1 article (11/2011)|
|4.||Sampath, Srirangan: 1 article (11/2011)|
|5.||Phillips, Jennifer B: 1 article (11/2011)|
|6.||Williams, David S: 1 article (11/2011)|
|7.||Washbourne, Philip: 1 article (11/2011)|
|8.||Mishra, Monalisa: 1 article (11/2011)|
|9.||Keats, Bronya J: 1 article (11/2011)|
|10.||Titus, Tom A: 1 article (11/2011)|
|1.||Deafness (Deaf Mutism)
06/01/1998 - "A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene."
03/31/2006 - "Mutations in the actin bundling and PDZ domain-containing protein harmonin are the causes of Usher syndrome type 1C (USH1C), a syndrome of congenital deafness and progressive blindness, as well as certain forms of non-syndromic deafness. "
07/01/2002 - "We have recently shown that USH1C underlies Usher syndrome type 1c (USH1C), an USH1 subtype characterized by profound deafness, retinitis pigmentosa, and vestibular dysfunction. "
|2.||Usher Syndromes (Usher Syndrome)
|3.||Hearing Loss (Hearing Impairment)
|4.||Retinitis Pigmentosa (Pigmentary Retinopathy)
06/01/1996 - "The Usher syndrome type 1C (USH1C) and familial hyperinsulinism (HI) loci have been assigned to chromosome 11p14-15.1, within the interval D11S419-D11S1310. "
06/01/1996 - "Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1."
|1.||Nonsense Codon (Nonsense Mutation)