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Volumn 291, Issue 5506, 2001, Pages 1040-1043
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An hPer2 phosphorylation site mutation in familial advanced sleep phase syndrome
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Author keywords
[No Author keywords available]
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Indexed keywords
CASEIN KINASE;
GLYCINE;
SERINE;
ARTICLE;
AUTOSOMAL DOMINANT DISORDER;
CHROMOSOME 2Q;
CIRCADIAN RHYTHM;
CONTROLLED STUDY;
FAMILIAL DISEASE;
FEMALE;
GENE LOCATION;
GENE LOCUS;
GENE MAPPING;
GENE MUTATION;
HUMAN;
HUMAN CELL;
MALE;
MISSENSE MUTATION;
NONHUMAN;
NUCLEOTIDE SEQUENCE;
PRIORITY JOURNAL;
PROTEIN PHOSPHORYLATION;
SLEEP DISORDER;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
ANIMALS;
BINDING SITES;
BIOLOGICAL CLOCKS;
CASEIN KINASES;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 2;
CIRCADIAN RHYTHM;
EXONS;
FEMALE;
GLYCINE;
HUMANS;
LINKAGE (GENETICS);
MALE;
MOLECULAR SEQUENCE DATA;
MUTATION, MISSENSE;
NUCLEAR PROTEINS;
PEDIGREE;
PHOSPHORYLATION;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
PROTEIN KINASES;
PROTEINS;
SERINE;
SLEEP DISORDERS, CIRCADIAN RHYTHM;
TRANSCRIPTION FACTORS;
ALAUDIDAE;
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EID: 0035136677
PISSN: 00368075
EISSN: None
Source Type: Journal
DOI: 10.1126/science.1057499 Document Type: Article |
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Times cited : (1244)
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References (38)
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