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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 Xu
Published 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.
Keyphrases
  • intellectual disability
  • copy number
  • genome wide
  • genome wide identification
  • dna methylation
  • autism spectrum disorder
  • genome wide analysis