A novel SSCP variant (c.828G>A) within the M2 domain of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene, CHRNA4

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Published in:Human mutation 2000-11, Vol.16 (5), p.450-450
Main Authors: Akiyoshi, H, Iwata, H, Fukuma, G, Yonetani, M, Wada, K, Kaneko, S, Mitsudome, A, Hirose, S
Format: Article
Language:English
Subjects:
Adenine
Epilepsies, Partial - genetics
Epilepsy, Frontal Lobe - genetics
Genetic Variation
Guanine
Humans
Neurons - metabolism
Polymorphism, Single-Stranded Conformational
Protein Structure, Tertiary
Receptors, Nicotinic - chemistry
Receptors, Nicotinic - genetics
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container_end_page 450
container_issue 5
container_start_page 450
container_title Human mutation
container_volume 16
creator Akiyoshi, H
Iwata, H
Fukuma, G
Yonetani, M
Wada, K
Kaneko, S
Mitsudome, A
Hirose, S
description
doi_str_mv 10.1002/1098-1004(200011)16:5<450::AID-HUMU27>3.0.CO;2-4
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subjects Adenine
Epilepsies, Partial - genetics
Epilepsy, Frontal Lobe - genetics
Genetic Variation
Guanine
Humans
Neurons - metabolism
Polymorphism, Single-Stranded Conformational
Protein Structure, Tertiary
Receptors, Nicotinic - chemistry
Receptors, Nicotinic - genetics
title A novel SSCP variant (c.828G>A) within the M2 domain of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene, CHRNA4
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