Putative founder effect in the Polish, Iranian and United States populations for the L144S SOD1 mutation associated with slowly uniform phenotype of amyotrophic lateral sclerosis

Epidemiology of amyotrophic lateral sclerosis

(2019) Elisa Longinetti et al.   CURRENT OPINION IN NEUROLOGY

Genetic analysis of patients with familial and sporadic amyotrophic lateral sclerosis in a Brazilian Research Center

(2016) Gerson Chadi et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis

(2013) Magdalena Kuźma-Kozakiewicz et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Development of a Smartphone App for a Genetics Website: The Amyotrophic Lateral Sclerosis Online Genetics Database (ALSoD)

(2013) Olubunmi Abel et al.   JMIR mHealth and uHealth

Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients

(2012) Afagh Alavi et al.   NEUROBIOLOGY OF AGING

Hereditary motor neuron disease in a large Norwegian family with a “H46R” substitution in the superoxide dismutase 1 gene

(2012) Rune Østern et al.   NEUROMUSCULAR DISORDERS

Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family

(2011) Mariusz Berdyński et al.   Amyotrophic Lateral Sclerosis

Genetic modifiers of neurological disease

(2011) Jennifer A Kearney   CURRENT OPINION IN GENETICS & DEVELOPMENT

ALS patients with SOD1 mutations in Switzerland show very diverse phenotypes and extremely long survival: Table 1

(2011) M Weber et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Age and founder effect of SOD1 A4V mutation causing ALS

(2009) M. Saeed et al.   NEUROLOGY