Associated Papers
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.
Kröll-Hermi A et al.
American Journal of Human Genetics, 2025
Loss-of-function mutation in PRMT9 causes abnormal synapse development by dysregulation of RNA alternative splicing.
Shen L et al.
Nature Communications, 2024
Genetics of recessive cognitive disorders.
Musante L et al.
Trends in Genetics : Tig, 2014
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
Najmabadi H et al.
Nature, 2011
Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1).
Anedda F et al.
Plos One, 2011
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