Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families
Article in Iranian Journal of Child Neurology (January 2022)
The most recent citing publications are shown below. View all 13 publications that cite this research output on Dimensions.
A Novel BBS9 Mutation Identified via Whole-Exome Sequencing in a Chinese Family with Bardet-Biedl Syndrome
Article in BioMed Research International (October 2021)
Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome
Article in BioMed Research International (February 2021)