✦ LIBER ✦

Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in CuZn superoxide dismutase gene: A possible new subtype of familial ALS

✍ Scribed by Masashi Aoki; Masahito Ogasawara; Yoichi Matsubara; Kuniaki Narisawa; Shozo Nakamura; Yasuto Itoyama; Koji Abe

Book ID: 118931979
Publisher: Elsevier Science
Year: 1994
Tongue: English
Weight: 644 KB
Volume: 126
Category: Article
ISSN: 0022-510X
DOI: 10.1016/0022-510x(94)90097-3

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel two-base mutation in the CuZn su

A novel two-base mutation in the CuZn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis in Japan

✍ Mitsuya Morita; Masashi Aoki; Koji Abe; Takafumi Hasegawa; Ryo Sakuma; Yoshiaki 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 307 KB

Mutations in Cu/Zn superoxide dismutase

Mutations in Cu/Zn superoxide dismutase (SOD1) are associated with familial amyotrophic lateral sclerosis (ALS)

✍ Robert H. Brown Jr. 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 45 KB

Molecular Analyses of the Cu/Zn Superoxi

Molecular Analyses of the Cu/Zn Superoxide Dismutase Gene in Patients with Familial Amyotrophic Lateral Sclerosis (ALS) in Japan

✍ Masashi Aoki; Koji Abe; Yasuto Itoyama 📂 Article 📅 1998 🏛 Springer 🌐 English ⚖ 573 KB

Mutations in Cu/Zn superoxide dismutase

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

✍ Rosen, Daniel R.; Siddique, Teepu; Patterson, David; Figlewicz, Denise A.; Sapp, 📂 Article 📅 1993 🏛 Nature Publishing Group 🌐 English ⚖ 488 KB

Novel 4-bp insertion in exon 5 of the Cu

Novel 4-bp insertion in exon 5 of the CuZn-superoxide dismutase (SOD1) gene associated with familial amyotrophic lateral sclerosis

✍ Claus Hansen; Ole Gredal; Lene Werdelin; Peter M. Andersen; Stefan L. Marklund; 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 228 KB

Mutations in the gene for low density lipoprotein receptor (LDL-R) lead to a disorder called familial hypercholesterolemia (FH). Affected individuals are characterized by increased levels of cholesterol in plasma, tendinous xanthomas, arcus lipoides corneae, and premature coronary heart disease. Up

Identification of three novel mutations

Identification of three novel mutations in the gene for CuZn superoxide dismutase in patients with familial amyotrophic lateral sclerosis

✍ Peter C Sapp; Daniel R Rosen; Betsy A Hosler; Jesus Esteban; Diane McKenna-Yasek 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 541 KB