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Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial amyotrophic lateral sclerosis with the homozygous mutation

✍ Scribed by Masaaki Kato; Masashi Aoki; Michiya Ohta; Makiko Nagai; Fumiko Ishizaki; Shigenobu Nakamura; Yasuto Itoyama

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Identification of a novel mutation in Cu

✍ A. Naini; O. Musumeci; L. Hayes; F. Pallotti; M. Del Bene; H. Mitsumoto 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 83 KB

A clinical variance in familial amyotrop

✍ R. Sakuma; K. Abe; M. Aoki; M. Ikeda; N. Okita; M. Hiwatari; M. Sakurai; Y. Itoy 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 595 KB

A novel mutation (Cys6Gly) in the Cu/Zn

✍ Satoshi Kohno; Yoshitomo Takahashi; Hiroaki Miyajima; Masahiro Serizawa; Koichi 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 160 KB

Clinical features and neuropathological

✍ Takekazu Ohi; Kyoko Saita; Shinji Takechi; Kazuki Nabesima; Hirofumi Tashiro; Ka 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 244 KB

Mutational analysis of the Cu/Zn superox

✍ Aguirre, Tania; Matthijs, Gert; Robberecht, Wim; Tilkin, Petra; Cassiman, Jean-J 📂 Article 📅 1999 🏛 Nature Publishing Group 🌐 English ⚖ 186 KB

Superoxide dismutase 1: Identification o

✍ Markus Kostrzewa; Maxwell S. Damian; U. Müller 📂 Article 📅 1996 🏛 Springer 🌐 English ⚖ 42 KB