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Q55059337-8A12E6F4-1C7C-41EE-8EDA-B67AA60F0650
Q55059337-8A12E6F4-1C7C-41EE-8EDA-B67AA60F0650
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55059337-8A12E6F4-1C7C-41EE-8EDA-B67AA60F0650
A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability.
P2860
Q55059337-8A12E6F4-1C7C-41EE-8EDA-B67AA60F0650
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55059337-8A12E6F4-1C7C-41EE-8EDA-B67AA60F0650
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type
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wasDerivedFrom
65339aec450bcdfa8b2f4ede7fbd4f22c71e811b
P2860
Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apnea