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Volumn 65, Issue 12, 2005, Pages 1995-
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A variant in the HS1-BP3 gene is associated with familial essential tremor [1]
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
ALANINE;
GLUTAMINE;
LEUCINE;
PROLINE;
HS1BP3 PROTEIN, HUMAN;
NERVE PROTEIN;
ALLELE;
AMINO ACID SUBSTITUTION;
CHROMOSOME 2P;
ESSENTIAL TREMOR;
FAMILIAL DISEASE;
GENE;
GENE LINKAGE DISEQUILIBRIUM;
GENE SEQUENCE;
GENETIC ASSOCIATION;
GENETIC LINKAGE;
GENETIC POLYMORPHISM;
GENETIC SCREENING;
GENETIC VARIABILITY;
HS1 BP3 GENE;
HUMAN;
LETTER;
PRIORITY JOURNAL;
RARE DISEASE;
CHROMOSOME 2;
CHROMOSOME MAP;
GENETIC PREDISPOSITION;
GENETICS;
GENOTYPE;
HAPLOTYPE;
INHERITANCE;
NOTE;
NUCLEOTIDE SEQUENCE;
AMINO ACID SUBSTITUTION;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 2;
DNA MUTATIONAL ANALYSIS;
ESSENTIAL TREMOR;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC SCREENING;
GENOTYPE;
HAPLOTYPES;
HUMANS;
INHERITANCE PATTERNS;
LINKAGE DISEQUILIBRIUM;
NERVE TISSUE PROTEINS;
POLYMORPHISM, GENETIC;
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EID: 33645730896
PISSN: 00283878
EISSN: None
Source Type: Journal
DOI: 10.1212/01.wnl.0000200984.10076.e5 Document Type: Letter |
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Times cited : (32)
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References (0)
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