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Q48126211-DF5E5006-D34D-441E-BEDE-A1B903921E8B
Q48126211-DF5E5006-D34D-441E-BEDE-A1B903921E8B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48126211-DF5E5006-D34D-441E-BEDE-A1B903921E8B
A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy.
P2093
Q48126211-DF5E5006-D34D-441E-BEDE-A1B903921E8B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48126211-DF5E5006-D34D-441E-BEDE-A1B903921E8B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2ad080c3b62358a521eb2e39d3918273e2b2f243
P1545
5
http://www.w3.org/2001/XMLSchema#string
P2093
F Pontén
http://www.w3.org/2001/XMLSchema#string