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Q29147428-CE36586A-1BC0-4FDA-B64A-12733BC575F4
Q29147428-CE36586A-1BC0-4FDA-B64A-12733BC575F4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q29147428-CE36586A-1BC0-4FDA-B64A-12733BC575F4
Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability
P2860
Q29147428-CE36586A-1BC0-4FDA-B64A-12733BC575F4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q29147428-CE36586A-1BC0-4FDA-B64A-12733BC575F4
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wasDerivedFrom
df153093afec6165f99cbbbcfe8a2297817abc78
P2860
A subunit of eukaryotic translation initiation factor 2α-phosphatase (CreP/PPP1R15B) regulates membrane traffic.