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Q44189852-69ED7DDE-BC1D-44B4-9C32-F800A51DE007
Q44189852-69ED7DDE-BC1D-44B4-9C32-F800A51DE007
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Statement
http://www.wikidata.org/entity/statement/Q44189852-69ED7DDE-BC1D-44B4-9C32-F800A51DE007
Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1.
P2860
Q44189852-69ED7DDE-BC1D-44B4-9C32-F800A51DE007
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44189852-69ED7DDE-BC1D-44B4-9C32-F800A51DE007
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wasDerivedFrom
ca660066260c2b7fe04c5b36d5a7b17709fab609
P2860
Further Delineation of the Phenotype of Congenital Disorder of Glycosylation DPAGT1-CDG (CDG-Ij) Identified by Homozygosity Mapping.