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Q48126211-480E4FE5-90A3-4F4B-800F-E728EB129AB6
Q48126211-480E4FE5-90A3-4F4B-800F-E728EB129AB6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48126211-480E4FE5-90A3-4F4B-800F-E728EB129AB6
A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy.
P2860
Q48126211-480E4FE5-90A3-4F4B-800F-E728EB129AB6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48126211-480E4FE5-90A3-4F4B-800F-E728EB129AB6
rank
NormalRank
type
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Statement
wasDerivedFrom
59ae212091375e83c63227546ce1b1b8597db026
P2860
Meckel-Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe