共 50 条
- [42] Molecular basis of deafness due to mutations in the connexin26 gene (GJB2) GAP JUNCTIONS: MOLECULAR BASIS OF CELL COMMUNICATION IN HEALTH AND DISEASE, 2000, 49 : 483 - 508
- [46] Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2012, 1818 (08): : 2014 - 2019
- [49] Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome BMC MEDICAL GENETICS, 2013, 14