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Q30525587-2E615BBB-4860-4497-A957-9E48A48C9B08
Q30525587-2E615BBB-4860-4497-A957-9E48A48C9B08
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http://www.wikidata.org/entity/statement/Q30525587-2E615BBB-4860-4497-A957-9E48A48C9B08
De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicine.
P2860
Q30525587-2E615BBB-4860-4497-A957-9E48A48C9B08
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30525587-2E615BBB-4860-4497-A957-9E48A48C9B08
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4af47260a6fdb8f5a2ab94a3b7657231e4ec937a
P2860
Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes