✦ LIBER ✦

Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis

✍ Scribed by Kim, Hee-Jung; Kwon, Min-Jung; Choi, Won-Jun; Oh, Ki-Wook; Oh, Seong-il; Ki, Chang-Seok; Kim, Seung Hyun

Book ID: 122290810
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 170 KB
Volume: 35
Category: Article
ISSN: 0197-4580
DOI: 10.1016/j.neurobiolaging.2014.03.001

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutations in UBQLN2 are rare in French a

Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis

✍ Stéphanie Millecamps; Philippe Corcia; Cécile Cazeneuve; Séverine Boillée; Danie 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 345 KB

UBQLN2 mutations are rare in French and

UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis

✍ Hussein Daoud; Hamid Suhail; Anna Szuto; William Camu; Francois Salachas; Vincen 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 876 KB

PFN1 mutations are rare in Han Chinese p

PFN1 mutations are rare in Han Chinese populations with amyotrophic lateral sclerosis

✍ Chen, YongPing; zheng, Zhen-Zhen; Huang, Rui; Chen, Ke; Song, Wei; Zhao, Bi; Che 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 322 KB

A novel SOD1 gene mutation in a Korean f

A novel SOD1 gene mutation in a Korean family with amyotrophic lateral sclerosis

✍ Nam-Hee Kim; Hyun-Jung Kim; Manho Kim; Kwang-Woo Lee 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 154 KB

SOD1 gene mutations in Italian patients

SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)

✍ L. Corrado; S. D’Alfonso; L. Bergamaschi; L. Testa; M. Leone; N. Nasuelli; P. Mo 📂 Article 📅 2006 🏛 Elsevier Science 🌐 English ⚖ 84 KB

Copper and zinc levels in familial amyot

Copper and zinc levels in familial amyotrophic lateral sclerosis patients with cuznsod gene mutations

✍ A. Radunović; H. T. Delves; W. Robberecht; P. Tilkin; Z. E. Enayat; C. E. Shaw; 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB 👁 2 views

to worsening of parkinsonian symptoms. Because Verhagen and co-workers [3] do not provide confirmation of their lesion locations, it is conceivable that their lesions encroached on the GPe. The second point raised by Krack and colleagues, is not really relevant, since it seems to apply solely to DB