World Of Taxonomy
C214859Level 9

Amyotrophic Lateral Sclerosis 26, with or without Frontotemporal Dementia

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant form of amyotrophic lateral sclerosis caused by mutation(s) in the TIA1 gene, encoding cytotoxic granule associated RNA binding protein TIA1.

**Synonyms:** - ALS26

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