Familial amyotrophic lateral sclerosis with novel A4DSOD1mutation with late age at onset and rapid progressive course-Reference-Cited by-同舟云学术

Familial amyotrophic lateral sclerosis with novel A4DSOD1mutation with late age at onset and rapid progressive course

Published:2013-01 Issue:1 Volume:1 Page:45-47
ISSN:2049-4173
Container-title:Neurology and Clinical Neuroscience
language:en
Short-container-title:Neurol Clin Neurosci

Author:

Naruse Hiroya¹,Iwata Atsushi,Takahashi Yuji¹,Ichihara Kazuaki²,Kamei Satoshi²,Yamatoku Masato³,Hirayama Toshikazu³,Suzuki Naoki⁴,Aoki Masashi⁴,Miyagawa Toji¹,Shimizu Jun¹,Tsuji Shoji¹,Goto Jun¹

Affiliation:

1. Department of Neurology; The University of Tokyo; Tokyo; Japan

2. Division of Neurology; Department of Medicine; Nihon University School of Medicine; Tokyo; Japan

3. Department of Neurology; St. Marianna University School of Medicine; Kawasaki; Kanagawa; Japan

4. Department of Neurology; Tohoku University School of Medicine; Aoba; Sendai; Japan

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference6 articles.

1. Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene;Andersen;Curr. Neurol. Neurosci. Rep.,2006

2. A mutation database for amyotrophic lateral sclerosis;Yoshida;Hum. Mutat.,2010

3. Prognosis in familial amyotrophic lateral sclerosis: progression and survival in patients with glu100gly and ala4 val mutations in Cu,Zn superoxide dismutase;Juneja;Neurology,1997

4. Instability of mutant Cu/Zn superoxide dismutase (Ala4Thr) associated with familial amyotrophic lateral sclerosis;Nakano;Neurosci. Lett.,1996

5. Rapid disease progression correlates with instability of mutant SOD1 in familial ALS;Sato;Neurology,2005

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