Article
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 - 1 Dec 2000
Bonati M T, Duga S, Asselta R, Ferini-Strambi L, Oldani A, Zucconi M, Malcovati M, Dalprà L, Tenchini M L
Abstract excerpt
A new polymorphism in intron 1 of the neuronal nicotinic acetylcholine receptor alpha 4 subunit gene (CHRNA4) was identified. It consists of a G to T substitution located in the downstream flanking region of a previously reported CA repeat marker. This polymorphism whose frequency is about six percent in a control population occurs near the 3' end of the reverse primer generally used to type the CA repeat marker....
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