Article
Scrutinizing the molecular, biochemical, and cytogenetic attributes in subjects with Rett syndrome (RTT) and their mothers.
Epilepsy & behavior : E&B - 1 Oct 2020
Meyyazhagan Arun, Balasubramanian Balamuralikrishnan, Kathannan Sankar, Alagamuthu Karthick Kumar, Easwaran Murugesh, Shanmugam Sureshkumar, Pappusamy Manikantan, Bhotla Haripriya Kuchi, Mustaqahamed Shafiahammedkhan, Arumugam Vijaya Anand, Kaul Tanushri, Keshavarao Sasikala
Abstract excerpt
Rett syndrome (RTT) is a stern dominant progressive neurological development disorder linked with X chromosome ranking second for mental slowdown, exclusively in females after few months of birth with normal development and growth period. Genetically any defects in universally expressed methyl-CpG binding protein 2 (MeCP2) transcription regulator gene are considered as radix for RTT in almost all the previous...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.