Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene-Reference-Cited by-同舟云学术

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Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene

Published:1997-11 Issue:5 Volume:61 Page:1078-1087
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Yue Qing,Jen Joanna C.,Nelson Stanley F.,Baloh Robert W.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference39 articles.

1. Episodic ataxia results from voltage-dependent potassium channels with altered functions;Adelman;Neuron,1995

2. Familial periodic cerebellar ataxia: a problem of intracellular pH homeostasis;Bain;Ann Neurol,1992

3. On-line analysis of eye movements using a digital computer;Baloh;Aviat Space Environ Med,1980

4. Late cortical cerebellar atrophy: clinical and oculographic features;Baloh;Brain,1986

5. Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p;Baloh;Ann Neurol,1997

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