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Q41931303-971B5F50-8B60-46E2-869A-1782D1F29747
Q41931303-971B5F50-8B60-46E2-869A-1782D1F29747
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http://www.wikidata.org/entity/statement/Q41931303-971B5F50-8B60-46E2-869A-1782D1F29747
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.
P2860
Q41931303-971B5F50-8B60-46E2-869A-1782D1F29747
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41931303-971B5F50-8B60-46E2-869A-1782D1F29747
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wasDerivedFrom
075a1493cf7cc2705dcc70cefeeb0288ff103e08
P2860
Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.