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| Mendeliome v0.9252 | MAOB | Zornitza Stark Marked gene: MAOB as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v0.9252 | MAOB | Zornitza Stark Gene: maob has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v0.9252 | MAOB |
Zornitza Stark gene: MAOB was added gene: MAOB was added to Mendeliome. Sources: Expert Review Mode of inheritance for gene: MAOB was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: MAOB were set to 31700678 Phenotypes for gene: MAOB were set to Cerebral palsy Review for gene: MAOB was set to RED Added comment: Variants identified in 2 unrelated individuals with CP (with same variant also identified in unaffected monozygotic twin). Sources: Expert Review |
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