Entity

Time filter

Source Type


Yang Y.-J.,Hunan Childrens Research Institute HCRI | Hu Y.,Hunan Childrens Research Institute HCRI | Zhao R.,Hunan Childrens Research Institute HCRI | He X.,Hunan Childrens Research Institute HCRI | And 7 more authors.
Scientific World Journal | Year: 2015

Infantile cystinosis (IC) is a rare autosomal recessive disorder characterized by a defect in the lysosomal-membrane transport protein, cystinosin. It serves as a prototype for lysosomal transport disorders. To date, several CTNS mutations have been identified as the cause of the prototypic disease across different ethnic populations worldwide. However, in Asia, the CTNS mutation is very rarely reported. For the Chinese population, no literature on CTNS mutation screening for IC is available to date. In this paper, by using the whole exome sequencing and Sanger sequencing, we identified two novel CTNS splicing deletions in a Chinese IC family, one at the donor site of exon 6 of CTNS (IVS6+1, del G) and the other at the acceptor site of exon 8 (IVS8-1, del GT). These data give information for the genetic counseling of the IC that occurred in Chinese population. © 2015 Yong-jia Yang et al. Source

Discover hidden collaborations