Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia and frontotemporal dementia

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)
228 Downloads (Pure)

Fingerprint

Dive into the research topics of 'Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia and frontotemporal dementia'. Together they form a unique fingerprint.

Medicine and Dentistry

Neuroscience