共 50 条
- [21] Novel nonsense mutation of the EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia JOURNAL OF DERMATOLOGY, 2014, 41 (11): : 1014 - 1016
- [25] A novel splicing mutation of the FRMD7 gene in a Chinese family with X-linked congenital nystagmus MOLECULAR VISION, 2012, 18 (10-11): : 87 - 91
- [27] Loss of the SEDL gene product (Sedlin) causes X-linked spondyloepiphyseal dysplasia tarda: Identification of a molecular defect in a Japanese family AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 99 (04): : 328 - 330
- [30] A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia Journal of Genetics, 2015, 94 : 115 - 119