In Search Of The Causative Genetic / Molecular Events In Bardet Biedl Syndrome Patients Excluded For
33/19/2019-TF/Rare/BMS
ICMR
Jan. 6, 2020
Jan. 5, 2023
Three Year
Bardet Biedl Syndrome
None
None
The Objective of the proposed study is to identify the genetic cause in patients excluded for mutations in known candidate BBS genes , Evaluation of methylation status and sequence variants in precurs
BBS, epigenetics, miRNA variants, epistasis, methylation
None
41,53,354/-
Dr. Sarangapani Sripriya/None/SNONGC department of Genetics and molecular biology, Vision research foundation, Chennai