A new biallelic polymorphism in intron 1 of the CHRNA4 gene may cause erroneous genotyping of a closely linked CA repeat marker

Molecular and Cellular Probes

Volumn 14, Issue 6, 2000, Pages 373-380

  Bonati, M ^a   Duga, S ^a   Asselta, R ^a   Ferini Strambi, L ^a   Oldani, A ^a   Zucconi, M ^a   Malcovati, M ^a   Dalpra L ^a   Tenchini, M ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

ADNFLE; Haplotype; Linkage analysis; Neuronal nicotinic acetylcholine receptor 4 subunit gene; Polymorphism

Indexed keywords

MICROSATELLITE DNA; NICOTINIC RECEPTOR;

ALLELE; ALPHA CHAIN; ARTICLE; CHROMOSOME 20Q; ERROR; FRONTAL LOBE EPILEPSY; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC MARKER; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; HYBRIDIZATION; INTRON; MARKER GENE; PRIORITY JOURNAL; RECEPTOR BINDING; SEQUENCE ANALYSIS;

EID: 0034529922     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcpr.2000.0327     Document Type: Article

References (20)

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9. Ser252Phe and 776ins3 mutations in the CHRNA4 gene are rare in the Italian ADNFLE population
10. Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies
11. Refinement of the localization of the gene for neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) to human chromosome 20q13.2-q13.3
12. Detection of a Cfol polymorphism within exon 5 of the human neuronal nicotinic acetylcholine receptor α4 subunit gene (CHRNA4)
13. A fok1 polymorphism in the human neuronal nicotinic acetylcholine receptor α4 subunit gene
14. SSCP variants within the α4 subunit of the neuronal nicotinic acetylcholine receptor gene
15. Dinucleotide polymorphism in the first intron of the human neuronal nicotinic acetylcholine receptor α4 subunit gene (CHRNA4)
16. Exon-intron structure of the human neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4)
17. Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis
18. Gene deletions causing human genetic disease: Mechanisms of mutagenesis and the role of the local DNA sequence environment