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Q47708439-FE0490E4-D158-41AB-866D-50ED50426008
Q47708439-FE0490E4-D158-41AB-866D-50ED50426008
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-FE0490E4-D158-41AB-866D-50ED50426008
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P31
Q47708439-FE0490E4-D158-41AB-866D-50ED50426008
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47708439-FE0490E4-D158-41AB-866D-50ED50426008
rank
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type
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Statement
wasDerivedFrom
738e298fa5feaaca35d43475fcba1be052fe7717
P31
scholarly article