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| Dystonia - complex v0.16 | DCTN1 | Bryony Thompson Marked gene: DCTN1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dystonia - complex v0.16 | DCTN1 | Bryony Thompson Gene: dctn1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dystonia - complex v0.16 | DCTN1 |
Bryony Thompson gene: DCTN1 was added gene: DCTN1 was added to Dystonia - complex. Sources: Expert list Mode of inheritance for gene: DCTN1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: DCTN1 were set to 24343258 Phenotypes for gene: DCTN1 were set to Perry syndrome MIM#168605 Review for gene: DCTN1 was set to RED Added comment: Dystonia is reported in two out of eight cases in a single family. Sources: Expert list |
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