Novel PRMT7 mutation in a rare case of dysmorphism and intellectual disability-Reference-Cited by-同舟云学术

Novel PRMT7 mutation in a rare case of dysmorphism and intellectual disability

Published:2021-07-09 Issue:1 Volume:67 Page:19-26
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Poquérusse Jessie^ORCID,Whitford Whitney,Taylor Juliet,Alburaiky Salam,Snell Russell G.,Lehnert Klaus,Jacobsen Jessie C.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://www.nature.com/articles/s10038-021-00955-5.pdf

Reference48 articles.

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4. Di Lorenzo A, Bedford MT. Histone arginine methylation. FEBS Lett. 2011;585:2024–31.

5. Szewczyk MM, Ishikawa Y, Organ S, Sakai N, Li F, Halabelian L, et al. Pharmacological inhibition of PRMT7 links arginine monomethylation to the cellular stress response. Nat Commun. 2020;11:2396.

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