Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease (2002)
Rehm,Heidi L., Zhang,Duan-Sun, Brown,M. Christian, Burgess,Barbara, Halpin,Chris, Berger,Wolfgang, ...
Norrie disease is an X-linked recessive syndrome of blindness, deafness, and mental retardation. A knock-out mouse model with an Ndp gene disruption was studied. We examined the hearing phenotype,...
Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease (2002)
Rehm, Heidi L., Zhang, Duan-Sun, Brown, M. Christian, Burgess, Barbara, Halpin, Chris, Berger, Wolfgang, ...
Norrie disease is an X-linked recessive syndrome of blindness, deafness, and mental retardation. A knock-out mouse model with an Ndp gene disruption was studied. We examined the hearing phenotype,...
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Snoeckx, Rikkert L., Huygen, Patrick L. M., Feldmann, Delphine, Marlin, Sandrine, Denoyelle, Françoise, Waligora, Jaroslaw, ...
Hearing impairment (HI) affects 1 in 650 newborns, which makes it the most common congenital sensory impairment. Despite extraordinary genetic heterogeneity, mutations in one gene, GJB2, which...
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Snoeckx, Rikkert L., Huygen, Patrick L. M., Feldmann, Delphine, Marlin, Sandrine, Denoyelle, Françoise, Waligora, Jaroslaw, ...
Hearing impairment (HI) affects 1 in 650 newborns, which makes it the most common congenital sensory impairment. Despite extraordinary genetic heterogeneity, mutations in one gene, GJB2, which...