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Q48126211-0D0D8A7A-10E3-4527-A246-B09951E389B6
Q48126211-0D0D8A7A-10E3-4527-A246-B09951E389B6
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Statement
http://www.wikidata.org/entity/statement/Q48126211-0D0D8A7A-10E3-4527-A246-B09951E389B6
A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy.
P2860
Q48126211-0D0D8A7A-10E3-4527-A246-B09951E389B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48126211-0D0D8A7A-10E3-4527-A246-B09951E389B6
rank
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type
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wasDerivedFrom
59ae212091375e83c63227546ce1b1b8597db026
P2860
Cep55 regulates spindle organization and cell cycle progression in meiotic oocyte.