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Q24680149-8613B084-1B6F-4067-A737-A77383B1665F
Q24680149-8613B084-1B6F-4067-A737-A77383B1665F
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http://www.wikidata.org/entity/statement/Q24680149-8613B084-1B6F-4067-A737-A77383B1665F
First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure
P2860
Q24680149-8613B084-1B6F-4067-A737-A77383B1665F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24680149-8613B084-1B6F-4067-A737-A77383B1665F
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wasDerivedFrom
8cc2dd72d7a4215509ca78ad398becc7bf170765
a6fae09a7c4fc1b224b6583dfc13abffc38e1a06
P2860
Cortical neuronal migration mutants suggest separate but intersecting pathways