4.1 Article

A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS

Related references

Note: Only part of the references are listed.
Article Geriatrics & Gerontology

De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients

Annemarie Huebers et al.

NEUROBIOLOGY OF AGING (2015)

Article Genetics & Heredity

SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotyp-phenotype correlations

Stephanie Millecamps et al.

JOURNAL OF MEDICAL GENETICS (2010)

Article Clinical Neurology

Incidence of amyotrophic lateral sclerosis in Europe

Giancarlo Logroscino et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)

Article Clinical Neurology

Natural history of young-adult amyotrophic lateral sclerosis

M. Sabatelli et al.

NEUROLOGY (2008)