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Q50858165-439978C2-BFBF-4A47-8BE9-9BCF7702B2FC
Q50858165-439978C2-BFBF-4A47-8BE9-9BCF7702B2FC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50858165-439978C2-BFBF-4A47-8BE9-9BCF7702B2FC
Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss.
P2860
Q50858165-439978C2-BFBF-4A47-8BE9-9BCF7702B2FC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50858165-439978C2-BFBF-4A47-8BE9-9BCF7702B2FC
rank
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wasDerivedFrom
bdf1328ef1febf319ebc081ead4f660db7b7d4d9
P2860
Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.