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Genes and Entities
OPTN
optineurin
OMIM:
602432
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Panel
Mode of inheritance
Details
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Adult onset neurodegenerative disorder
R-numbers:
R58
Signed-off version 7.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia, OMIM:613435