Linkage Disequilibrium at the Angelman Syndrome Gene UBE3A in Autism Families

Autistic disorder is a neurodevelopmental disorder with a complex genetic etiology. Observations of maternal duplications affecting chromosome 15q11–q13 in patients with autism and evidence for linkage and linkage disequilibrium to markers in this region in chromosomally normal autism families indic...

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Veröffentlicht in:	Genomics (San Diego, Calif.) Calif.), 2001-09, Vol.77 (1-2), p.105-113
Hauptverfasser:	Nurmi, Erika L., Bradford, Yuki, Chen, Yi-hui, Hall, Jenifer, Arnone, Brenda, Gardiner, Mary Beth, Hutcheson, Holli B., Gilbert, John R., Pericak-Vance, Margaret A., Copeland-Yates, Susan A., Michaelis, Ron C., Wassink, Thomas H., Santangelo, Susan L., Sheffield, Val C., Piven, Joseph, Folstein, Susan E., Haines, Jonathan L., Sutcliffe, James S.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alleles Angelman syndrome Angelman Syndrome - genetics Autistic Disorder - genetics Base Sequence Biological and medical sciences Chromosome Deletion Chromosomes, Human, Pair 15 - genetics DNA - chemistry DNA - genetics DNA Mutational Analysis Family Health Female Fundamental and applied biological sciences. Psychology GABRA5 gene GABRB3 gene GABRG3 gene Gene Frequency Genes. Genome Genotype Humans Ligases - genetics Linkage Disequilibrium Male Microsatellite Repeats Molecular and cellular biology Molecular genetics Molecular Sequence Data Polymorphism, Single Nucleotide Protein Subunits Receptors, GABA-A - genetics Sequence Deletion UBE3A gene Ubiquitin-Protein Ligases
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