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SNURF gene

Known as: SNRPN Upstream Reading Frame Gene, SNRPN upstream reading frame, SNURF 
This gene may be involved in cerebral development.
National Institutes of Health

Papers overview

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2016
2016
Prader–Willi syndrome is a rare syndrome characterized by hypotonia, developmental delay and excessive appetite. This syndrome is… 
2003
2003
Die Region 15q11-q13 enthalt zwei unterschiedlich gepragte Gencluster, die der koordinierten Kontrolle eines Imprinting-Centers…