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| Genetic Epilepsy v0.2196 | LMX1B | Elena Savva Marked gene: LMX1B as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2196 | LMX1B | Elena Savva Gene: lmx1b has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2196 | LMX1B |
Elena Savva gene: LMX1B was added gene: LMX1B was added to Genetic Epilepsy. Sources: Literature Mode of inheritance for gene: LMX1B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: LMX1B were set to Focal segmental glomerulosclerosis 10 MIM#256020; Nail-patella syndrome MIM#161200 Review for gene: LMX1B was set to RED Added comment: GeneReviews - Epilepsy was reported in 6% of affected individuals in one large study [Sweeney et al 2003]. No new literature describing SNVs in this gene and epilepsy/seizures. Gene was listed on Oliver's list Sources: Literature |
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