NOP56_GGCCTGTT

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list NOP56_GGCCTGTT STR in Hereditary neuropathy

Level 3: Motor and Sensory Disorders of the PNS
Level 2: Neurology and neurodevelopmental disorders
Version 1.477

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Removed
  • Expert list
Phenotypes
  • Spinocerebellar ataxia 36, OMIM:614153
Tags
  • STR
  • curated_removed