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| Speech apraxia v0.37 | TRIP12 | Zornitza Stark Marked gene: TRIP12 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Speech apraxia v0.37 | TRIP12 | Zornitza Stark Gene: trip12 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Speech apraxia v0.37 | TRIP12 | Zornitza Stark Classified gene: TRIP12 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Speech apraxia v0.37 | TRIP12 | Zornitza Stark Gene: trip12 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Speech apraxia v0.31 | TRIP12 |
Thomas Scerri gene: TRIP12 was added gene: TRIP12 was added to Speech apraxia. Sources: Expert list,Expert Review Mode of inheritance for gene: TRIP12 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TRIP12 were set to 36117209 Phenotypes for gene: TRIP12 were set to Intellectual developmental disorder, autosomal dominant 49, MIM# 617752 Review for gene: TRIP12 was set to RED Added comment: First reported CAS case with a de novo exon duplication of TRIP12 (Kaspi et al., 2022; PMID: 36117209). Sources: Expert list, Expert Review |
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