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Q36903600-77011B19-B2BB-4E98-B3F0-51CDFCC7CB4C
Q36903600-77011B19-B2BB-4E98-B3F0-51CDFCC7CB4C
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Statement
http://www.wikidata.org/entity/statement/Q36903600-77011B19-B2BB-4E98-B3F0-51CDFCC7CB4C
Electroclinical Features of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation (CDGs)
P2860
Q36903600-77011B19-B2BB-4E98-B3F0-51CDFCC7CB4C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36903600-77011B19-B2BB-4E98-B3F0-51CDFCC7CB4C
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wasDerivedFrom
17a86fc66126dce363edca0d05136f7e4e99f109
P2860
29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype