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cadcc6c385bbdbe7b746db27e44f7dd139e15bd7
cadcc6c385bbdbe7b746db27e44f7dd139e15bd7
Reference
http://www.wikidata.org/reference/cadcc6c385bbdbe7b746db27e44f7dd139e15bd7
Q55782425-9F88FFD1-EE73-466B-BF05-95B491364EB4
Q55782425-B9DA73D2-2973-456C-BBE0-C1B2A0F1FD7E
wasDerivedFrom
cadcc6c385bbdbe7b746db27e44f7dd139e15bd7
Reference
http://www.wikidata.org/reference/cadcc6c385bbdbe7b746db27e44f7dd139e15bd7
type
Reference
P248
AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis