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Q47708439-fa223720-47f5-e4e6-2b5e-aa4a520f9a92
Q47708439-fa223720-47f5-e4e6-2b5e-aa4a520f9a92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-fa223720-47f5-e4e6-2b5e-aa4a520f9a92
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P921
Q47708439-fa223720-47f5-e4e6-2b5e-aa4a520f9a92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-fa223720-47f5-e4e6-2b5e-aa4a520f9a92
rank
NormalRank
type
BestRank
Statement
P921
ASPM