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Volumn 112, Issue 5-6, 2003, Pages 619-620
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Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia
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Author keywords
[No Author keywords available]
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Indexed keywords
ALLELE;
ATAXIA;
BRADYKINESIA;
BRAIN ATROPHY;
BRAIN SCINTISCANNING;
CEREBELLUM ATROPHY;
CLINICAL FEATURE;
COHORT ANALYSIS;
COMPUTER ASSISTED TOMOGRAPHY;
DEGENERATIVE DISEASE;
DELIVERY;
DIAGNOSTIC PROCEDURE;
DISEASE ASSOCIATION;
DYSARTHRIA;
DYSTONIA;
FEMALE;
FRAGILE X GENE;
GAIT DISORDER;
GENE;
GENE MUTATION;
GENETIC ANALYSIS;
HEARING IMPAIRMENT;
HETEROZYGOTE;
HUMAN;
INCIDENCE;
LETTER;
MALE;
MUSCLE RIGIDITY;
NEUROLOGIC DISEASE;
NUCLEAR MAGNETIC RESONANCE IMAGING;
NYSTAGMUS;
OVARY INSUFFICIENCY;
PHENOTYPE;
POPULATION;
PREGNANCY;
PRIORITY JOURNAL;
SEIZURE;
SENSORY DYSFUNCTION;
SPINOCEREBELLAR DEGENERATION;
TENDON REFLEX;
WHITE MATTER;
X CHROMOSOME;
ADULT;
AGED;
CHILD;
FRAGILE X SYNDROME;
GENETICS;
MIDDLE AGED;
MUTATION;
PATHOPHYSIOLOGY;
TRINUCLEOTIDE REPEAT;
ATAXIA;
ADULT;
AGED;
CHILD;
FRAGILE X SYNDROME;
HUMANS;
MALE;
MIDDLE AGED;
MUTATION;
SPINOCEREBELLAR ATAXIAS;
TRINUCLEOTIDE REPEAT EXPANSION;
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EID: 0038281167
PISSN: 03406717
EISSN: None
Source Type: Journal
DOI: 10.1007/s00439-003-0939-z Document Type: Letter |
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Times cited : (75)
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References (4)
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