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Q36433297-21AD56E9-E89F-4411-A04E-AE2D4BEB880B
Q36433297-21AD56E9-E89F-4411-A04E-AE2D4BEB880B
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http://www.wikidata.org/entity/statement/Q36433297-21AD56E9-E89F-4411-A04E-AE2D4BEB880B
Further Delineation of the Phenotype of Congenital Disorder of Glycosylation DPAGT1-CDG (CDG-Ij) Identified by Homozygosity Mapping.
P2860
Q36433297-21AD56E9-E89F-4411-A04E-AE2D4BEB880B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36433297-21AD56E9-E89F-4411-A04E-AE2D4BEB880B
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wasDerivedFrom
2addffeafbf7faa6a07c4c79aa69b379e8df4d5c
P2860
Actin mutations are one cause of congenital fibre type disproportion.