Dinucleotide polymorphism in the first intron of the human neuronal nicotinic acetylcholine receptor α4 subunit gene (CHRNA4)

Clinical Genetics

Volumn 50, Issue 5, 1996, Pages 433-434

  Weiland, S ^a   Steinlein, O ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER; NICOTINIC RECEPTOR; RECEPTOR SUBUNIT;

ARTICLE; CHROMOSOMAL LOCALIZATION; CONTROLLED STUDY; DNA POLYMORPHISM; GENE LOCUS; HUMAN; HUMAN CELL; INTRON; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

EID: 0030460135     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb02403.x     Document Type: Article

References (4)

1. Budowle B, Chakraborty R, Giusti AM, Eisenberg AJ, Allen RC. Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE. Am J Hum Genet 1991: 48: 137-144.
2. Steinlein O, Smigrodzki R, Lindstrom J, Anand R, Köhler M, Tocharoentanaphol C, Vogel F. Refinement of the localization of the gene for neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) to human chromosome 20q13.2-q13.3. Genomics 1994: 22: 493-495.
3. Steinlein O, Mulley JC, Propping P, Wallace RH, Phillips HA, Sutherland GR, Scheffer I, Berkovic SF. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy. Nature Genet 1995: 11: 201-203.
4. Steinlein O, Weiland S, Stoodt J, Propping P. Exon-intron structure of the human neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4). Genomics 1996: 32: 289-294.