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Q47708439-C2B035BA-3549-4DB9-97C5-CB54E31CF2F9
Q47708439-C2B035BA-3549-4DB9-97C5-CB54E31CF2F9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-C2B035BA-3549-4DB9-97C5-CB54E31CF2F9
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P1476
Q47708439-C2B035BA-3549-4DB9-97C5-CB54E31CF2F9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-C2B035BA-3549-4DB9-97C5-CB54E31CF2F9
rank
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type
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wasDerivedFrom
738e298fa5feaaca35d43475fcba1be052fe7717
P1476
Whole exome sequencing identif
......
, primary, autosomal recessive
@en