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Amyotrophic Lateral Sclerosis Volume 8, 2007 - Issue 2
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ORIGINAL ARTICLE

Clinical characteristics of familial amyotrophic lateral sclerosis with a Phe20Cys mutation in the SOD1 gene in a Korean family

Hyun Young Kim Department of Neurology, College of Medicine, Hanyang University, Seoul
,
Chang‐Seok Ki Department of Laboratory Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul
,
Seong‐Ho Koh Department of Neurology, College of Medicine, Hanyang University, Seoul
,
Kee‐Hyung Park Department of Neurology, Gachon University Gil Medical Center, Inchon
,
Il‐Nam Sunwoo Department of Neurology, College of Medicine, Yonsei University, Seoul, South Korea
&
Seung H. Kim Department of Neurology, College of Medicine, Hanyang University, SeoulCorrespondence[email protected]
Pages 73-78 | Received 09 Jun 2006, Accepted 10 Jun 2006, Published online: 10 Jul 2009

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. (2018) Theme 1 Genetics and genomics. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19:sup1, pages 91-111.
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Stefania Battistini, Claudia Ricci, Fabio Giannini, Silvia Calzavara, Giuseppe Greco, Alberto Del Corona, Michelangelo Mancuso, Noè Battistini, Gabriele Siciliano & Paola Carrera. (2010) G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype. Amyotrophic Lateral Sclerosis 11:1-2, pages 210-215.
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Articles from other publishers (6)

Victoria M. McLeod, Chew L. Lau, Mathew D.F. Chiam, Thusitha W. Rupasinghe, Ute Roessner, Elvan Djouma, Wah C. Boon & Bradley J. Turner. (2019) Androgen receptor antagonism accelerates disease onset in the SOD1 G93A mouse model of amyotrophic lateral sclerosis . British Journal of Pharmacology.
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Daniel Cacabelos, Omar Ramírez-Núñez, Ana Belén Granado-Serrano, Pascual Torres, Victòria Ayala, Victoria Moiseeva, Mònica Povedano, Isidre Ferrer, Reinald Pamplona, Manuel Portero-Otin & Jordi Boada. (2016) Early and gender-specific differences in spinal cord mitochondrial function and oxidative stress markers in a mouse model of ALS. Acta Neuropathologica Communications 4:1.
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Summer B. GibsonKarla P. FigueroaMark B. BrombergStefan-M. PulstLisa Cannon-Albright. (2014) Familial clustering of ALS in a population-based resource. Neurology 82:1, pages 17-22.
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Min-Jung Kwon, Wonki Baek, Chang-Seok Ki, Hyun Young Kim, Seong-Ho Koh, Jong-Won Kim & Seung Hyun Kim. (2012) Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS. Neurobiology of Aging 33:5, pages 1017.e17-1017.e23.
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Pamela A. McCombe & Robert D. Henderson. (2010) Effects of gender in amyotrophic lateral sclerosis. Gender Medicine 7:6, pages 557-570.
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Enrique Syriani, Miguel Morales & Josep Gamez. (2009) The p.E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time. Journal of the Neurological Sciences 285:1-2, pages 46-53.
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