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Q51919650-33FDC6F0-F120-493E-83BE-41E83A112D55
Q51919650-33FDC6F0-F120-493E-83BE-41E83A112D55
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51919650-33FDC6F0-F120-493E-83BE-41E83A112D55
Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndrome.
P2860
Q51919650-33FDC6F0-F120-493E-83BE-41E83A112D55
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51919650-33FDC6F0-F120-493E-83BE-41E83A112D55
rank
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Statement
wasDerivedFrom
c945ec88be7bc5ee46594d217bafb6ea918e86cb
P2860
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.