SSCP variants within the α4 subunit of the neuronal nicotinic acetylcholine receptor gene

Clinical Genetics

Volumn 51, Issue 2, 1997, Pages 135-136

  Phillips, Hilary A ^a   Mulley, John C ^a  

^a WOMEN S AND CHILDREN S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

NICOTINIC RECEPTOR;

ARTICLE; CHOLINERGIC TRANSMISSION; CHROMOSOME; FRONTAL LOBE EPILEPSY; GENE LOCUS; HUMAN; PRIORITY JOURNAL; RECEPTOR GENE; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0030971230     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1997.tb02439.x     Document Type: Article

References (6)

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2. Phillips HA, Scheffer IE, Berkovic SF, Hollway GE, Sutherland GR, Mulley JC. Localisation of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2. Nature Genet 1995: 10: 117-118.
3. Steinlein O, Anokhin A, Yping M, Schalt E, Vogel F. Localization of a gene for the human low-voltage EEG on 20q and genetic heterogeneity. Genomics 1992: 12: 69-73.
4. Steinlein O, Mulley JC, Propping P, Wallace R, Phillips HA, Sutherland GR, Scheffer IE, 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.
5. Steinlein O, Smigrodzki R, Lindstrom J, Anand R, Köhler M, Tocharoentanaphol C, Vogel F. Refinement of the localisation of the gene for neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) to human chromosome 20q13.2-q13.3. Genomics 1994: 22: 493-495.
6. 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.