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Q47708439-38E2287D-286D-461C-89C0-8FE130DF31F2
Q47708439-38E2287D-286D-461C-89C0-8FE130DF31F2
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Statement
http://www.wikidata.org/entity/statement/Q47708439-38E2287D-286D-461C-89C0-8FE130DF31F2
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P2860
Q47708439-38E2287D-286D-461C-89C0-8FE130DF31F2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-38E2287D-286D-461C-89C0-8FE130DF31F2
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Statement
wasDerivedFrom
57472cfb47750e9e311ea8fddfb60937add6129f
P2860
Evolution of the human ASPM gene, a major determinant of brain size