Two Distinctively Rare Syndromes in a Case of Primary Amenorrhea: 18p Deletion and Mayer–Rokitansky–Kuster–Hauser Syndromes
Monika Anant(All India Institute of Medical Sciences), Ajit Kumar Saxena(Institute of Minerals and Materials Technology), Nutan Raj(All India Institute of Medical Sciences), Arun Prasad(Apollo Hospitals), Subhash Kumar(All India Institute of Medical Sciences Raipur), Neelu Yadav(HCG Cancer Centre)
Cited by 6
Related Papers
Small Molecule Regulators of Protein Arginine Methyltransferases
|Journal of Biological Chemistry|2004|334
The Novel Human Protein Arginine N-Methyltransferase PRMT6 Is a Nuclear Enzyme Displaying Unique Substrate Specificity
|Journal of Biological Chemistry|2002|331
Global burden of metabolic diseases, 1990–2021
|Metabolism|2024|294
Specific protein methylation defects and gene expression perturbations in coactivator-associated arginine methyltransferase 1-deficient mice
|Proceedings of the National Academy of Sciences|2003|282