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Q33909988-27388EAE-25BA-4E72-BA42-F4B3D2CE0F3C
Q33909988-27388EAE-25BA-4E72-BA42-F4B3D2CE0F3C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33909988-27388EAE-25BA-4E72-BA42-F4B3D2CE0F3C
The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome.
P2860
Q33909988-27388EAE-25BA-4E72-BA42-F4B3D2CE0F3C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33909988-27388EAE-25BA-4E72-BA42-F4B3D2CE0F3C
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wasDerivedFrom
55296de2b0ecec37c28ca7f5d75f55e9ff6925c1
P2860
Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation.