The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families.

Cited by papers we hold 2

• RNA modification: mechanisms and therapeutic targets · 2023
  No notice
• The mitochondrial epitranscriptome: the roles of RNA modifications in mitochondrial translation and human disease · 2017
  No notice

Reads

A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.