Xq27 FRAXA locus is a strong candidate for dyslexia: Evidence from a genome-wide scan in French families

Behavior Genetics

Volumn 43, Issue 2, 2013, Pages 132-140

  Huc Chabrolle, M ^a,b,f   Charon, C ^c   Guilmatre, A ^d   Vourc'H, P ^a,b   Tripi, G ^b,e   Barthez, M A ^b   Sizaret, E ^b   Thepault, R A ^a,b   Le Gallic, S ^d   Hager, J ^c   Toutain, A ^a,b   Raynaud, M ^a,b   Andres, C ^a,b   Campion, D ^d   Laumonnier, F ^a,b   Bonnet Brilhault, F ^a,b  

^a UNIVERSITÉ DE TOURS   (France)

^b University Hospitals of Tours   (France)

^c DIF   (France)

^d INSERM   (France)

^e UNIVERSITY OF PALERMO   (Italy)

^f CHU BRETONNEAU   (France)

Author keywords

Dyslexia; Dyx 9 loci; Fmr1; Linkage study; Multiplex families

Indexed keywords

3' UNTRANSLATED REGION; ADOLESCENT; ARTICLE; ASFMR1 GENE; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; CXORF1 GENE; CXORF51 GENE; DYSLEXIA; FEMALE; FMR1 GENE; FMR1NB GENE; FMR2 GENE; FRAXA GENE; GENE; GENE FUNCTION; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENETIC LINKAGE; HUMAN; LIMIT OF DETECTION; LINKAGE ANALYSIS; MALE; MUTATIONAL ANALYSIS; PHENOTYPIC VARIATION; SCORING SYSTEM; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SLITRK2 GENE; TRINUCLEOTIDE REPEAT;

CHILD; CHROMOSOMES, HUMAN, X; DYSLEXIA; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; FRANCE; GENES, X-LINKED; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; LOD SCORE; MALE; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84879417682     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-012-9575-5     Document Type: Article

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