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Q47708439-6B90B06D-A100-486A-9DE4-7C62FEC16F00
Q47708439-6B90B06D-A100-486A-9DE4-7C62FEC16F00
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-6B90B06D-A100-486A-9DE4-7C62FEC16F00
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P921
Q47708439-6B90B06D-A100-486A-9DE4-7C62FEC16F00
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-6B90B06D-A100-486A-9DE4-7C62FEC16F00
rank
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type
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Statement
P921
microcephaly