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Q34329643-5BED4BF4-0891-4C9D-92B1-61F20663F0F8
Q34329643-5BED4BF4-0891-4C9D-92B1-61F20663F0F8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34329643-5BED4BF4-0891-4C9D-92B1-61F20663F0F8
Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements
P2860
Q34329643-5BED4BF4-0891-4C9D-92B1-61F20663F0F8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34329643-5BED4BF4-0891-4C9D-92B1-61F20663F0F8
rank
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type
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Statement
wasDerivedFrom
63b8cf234556357ee02ad2deae9c6c55d261c27d
P2860
Mutations in EFHC1 cause juvenile myoclonic epilepsy