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Volumn 255, Issue 7, 2008, Pages 1097-1099
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Episodic ataxia: SLC1A3 and CACNB4 do not explain the apparent genetic heterogeneity
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Author keywords
[No Author keywords available]
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Indexed keywords
ACETAZOLAMIDE;
CALCIUM CHANNEL;
CALCIUM CHANNEL BETA 4 SUBUNIT;
EXCITATORY AMINO ACID TRANSPORTER 1;
UNCLASSIFIED DRUG;
ADOLESCENT;
ADULT;
ATAXIA;
AUTISM;
CLINICAL ARTICLE;
COGNITIVE DEFECT;
DEVELOPMENTAL DISORDER;
DYSTONIA;
EPISODIC ATAXIA TYPE 2;
FAMILIAL HEMIPLEGIC MIGRAINE;
FAMILY HISTORY;
FEMALE;
GENE;
GENETIC HETEROGENEITY;
HUMAN;
LEARNING DISORDER;
LETTER;
MALE;
MUTATIONAL ANALYSIS;
MYOCLONUS EPILEPSY;
NYSTAGMUS;
ONSET AGE;
PHENOTYPE;
PRIORITY JOURNAL;
SCHOOL CHILD;
ADOLESCENT;
ADULT;
ATAXIA;
CALCIUM CHANNELS;
CHILD;
DNA MUTATIONAL ANALYSIS;
EXCITATORY AMINO ACID TRANSPORTER 1;
FAMILY HEALTH;
FEMALE;
HUMANS;
MALE;
MIDDLE AGED;
MUTATION;
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EID: 50049109437
PISSN: 03405354
EISSN: 14321459
Source Type: Journal
DOI: 10.1007/s00415-008-0844-4 Document Type: Letter |
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Times cited : (11)
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References (6)
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