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Volumn 47, Issue 7, 2008, Pages 736-739
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Fragile X syndrome: Keys to the molecular genetics of synaptic plasticity
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Author keywords
[No Author keywords available]
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Indexed keywords
FRAGILE X MENTAL RETARDATION PROTEIN;
CYTOSINE;
FMR1 PROTEIN, HUMAN;
GUANINE;
MESSENGER RNA;
AMINO ACID SEQUENCE;
ARTICLE;
DNA METHYLATION;
FMRI GENE;
FRAGILE X SYNDROME;
GENE;
GENE MUTATION;
HUMAN;
MENTAL DEFICIENCY;
NERVE CELL PLASTICITY;
PRIORITY JOURNAL;
PROTEIN MODIFICATION;
PROTEIN TARGETING;
SYNDROME DELINEATION;
CHILD;
DNA MICROARRAY;
EXON;
FEMALE;
GENETIC TRANSCRIPTION;
GENETICS;
HETEROZYGOTE DETECTION;
INTRON;
MALE;
METABOLISM;
NUCLEOTIDE REPEAT;
PROMOTER REGION;
TRINUCLEOTIDE REPEAT;
AMINO ACID SEQUENCE;
CHILD;
CYTOSINE;
EXONS;
FEMALE;
FRAGILE X MENTAL RETARDATION PROTEIN;
FRAGILE X SYNDROME;
GUANINE;
HETEROZYGOTE DETECTION;
HUMANS;
INTRONS;
MALE;
NEURONAL PLASTICITY;
OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS;
PROMOTER REGIONS (GENETICS);
REPETITIVE SEQUENCES, NUCLEIC ACID;
RNA, MESSENGER;
TRANSCRIPTION, GENETIC;
TRINUCLEOTIDE REPEATS;
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EID: 50549089689
PISSN: 08908567
EISSN: 15275418
Source Type: Journal
DOI: 10.1097/CHI.0b013e3181739619 Document Type: Article |
Times cited : (9)
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References (6)
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