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Q47708439-8F8068E0-D139-429B-8E5B-01EB085C2CBA
Q47708439-8F8068E0-D139-429B-8E5B-01EB085C2CBA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-8F8068E0-D139-429B-8E5B-01EB085C2CBA
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P1433
Q47708439-8F8068E0-D139-429B-8E5B-01EB085C2CBA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-8F8068E0-D139-429B-8E5B-01EB085C2CBA
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
738e298fa5feaaca35d43475fcba1be052fe7717
P1433
F1000Research