Clinical Diagnosis of X-Linked Spondyloepiphyseal Dysplasia Tarda and a Novel Missense Mutation in the Sedlin Gene (SEDL).
Lei KongDongxu WangShanshan LiChengsheng ZhangXiuyun JiangQingbo GuanZhenlin ZhangFei JingJin XuPublished in: International journal of endocrinology (2018)
SEDT in this family was caused by a G/C missense mutation in exon 6 of the SEDL gene, previously not shown to be associated with X-linked SEDT.