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MIM:614173 - JOUBERT SYNDROME 13; JBTS13
Xenbase Genes: tctn1
Human Disease Resource: MIM
MONDO:0013608 - Joubert syndrome 13 |
MONDO:0018772 - Joubert syndrome |
DOID:0110982 - Joubert syndrome 13 |
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MONDO:0013608 - Joubert syndrome 13 |
MONDO:0018772 - Joubert syndrome |
DOID:0110982 - Joubert syndrome 13 |