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Q28367963-37E2AE47-E01E-4CF8-8912-97E9C63D2BFF
Q28367963-37E2AE47-E01E-4CF8-8912-97E9C63D2BFF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28367963-37E2AE47-E01E-4CF8-8912-97E9C63D2BFF
A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease
P2860
Q28367963-37E2AE47-E01E-4CF8-8912-97E9C63D2BFF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28367963-37E2AE47-E01E-4CF8-8912-97E9C63D2BFF
rank
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type
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Statement
wasDerivedFrom
43ecf0279223fe3583a63adef8ce24aff4ef731d
P2860
A repeated element in the regulatory region of the MNK gene and its deletion in a patient with occipital horn syndrome