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Q34506328-36CED909-1D11-4F79-BB2C-BE14D820803B
Q34506328-36CED909-1D11-4F79-BB2C-BE14D820803B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34506328-36CED909-1D11-4F79-BB2C-BE14D820803B
Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome.
P2860
Q34506328-36CED909-1D11-4F79-BB2C-BE14D820803B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34506328-36CED909-1D11-4F79-BB2C-BE14D820803B
rank
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type
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wasDerivedFrom
5b449ba1c5a42a673dd81623bb1f335404e13dc8
P2860
Lack of collagen XVIII/endostatin results in eye abnormalities