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Long QT syndrome v1.26 | NOS1AP | Rebecca Whittington commented on gene: NOS1AP: [QT interval, variation in] (OMIM %610741) - only association | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Long QT syndrome v1.25 | NOS1AP | Rebecca Whittington commented on gene: NOS1AP: Not enough evidence for this gene. PMID:26132555. PMID: 20538168. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Long QT syndrome v1.24 | NOS1AP | Rebecca Whittington reviewed gene: NOS1AP: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: Unknown; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Long QT syndrome v1.16 | NOS1AP |
Ellen McDonagh Source South West GLH was added to NOS1AP. Mode of inheritance for gene NOS1AP was changed from to Unknown |