Authors:
Kunst, H
Huybrechts, C
Marres, H
Huygen, P
Van Camp, G
Cremers, C
Citation: H. Kunst et al., The phenotype of DFNA13/COL11A2: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment, AM J OTOL, 21(2), 2000, pp. 181-187
Authors:
McGuirt, WT
Prasad, SD
Griffith, AJ
Kunst, HPM
Green, GE
Shpargel, KB
Runge, C
Huybrechts, C
Mueller, RF
Lynch, E
King, MC
Brunner, HG
Cremers, CWRJ
Takanosu, M
Li, SW
Arita, M
Mayne, R
Prockop, DJ
Van Camp, G
Smith, RJH
Citation: Wt. Mcguirt et al., Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13), NAT GENET, 23(4), 1999, pp. 413-419