Familial spinocerebellar ataxia with cerebellar atrophy, peripheral neuropathy, and elevated level of serum creatine kinase, ?-globulin, and ?-fetoprotein-Reference-Cited by-同舟云学术

Familial spinocerebellar ataxia with cerebellar atrophy, peripheral neuropathy, and elevated level of serum creatine kinase, ?-globulin, and ?-fetoprotein

Published:1998-08 Issue:2 Volume:44 Page:265-269
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Watanabe Mitsunori,Sugai Yoshiro,Concannon Patrick,Koenig Michel,Schmitt Mich�Le,Sato Madoka,Shizuka Masami,Mizushima Kazuyuki,Ikeda Yoshio,Tomidokoro Yasushi,Okamoto Koichi,Shoji Mikio

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference19 articles.

1. Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

2. Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia

3. The Friedreich's ataxia gene encodes a novel phosphatidylinositol–4–phosphate 5–kinase

4. Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein

5. A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

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