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Journal Article
by Liu, ZM and Zhang, L and Shen, DM and Ding, CH and Yang, XY and Zhang, WH and Li, JW and Deng, J and Gong, S and Liu, J and Qian, SY and Fang, F
FRONTIERS IN PHARMACOLOGY, ISSN 1663-9812, 03/2019, Volume 10, p. 259
Congenital myasthenic syndromes (CMSs) are a group of inherited disorders caused by genetic defects in neuromuscular junctions. Mutations in CHAT, encoding... 
DIAGNOSIS | READ ALIGNMENT | episodic apnea | CHAT | severe | DISEASE | congenital myasthenic syndromes | PHARMACOLOGY & PHARMACY | large deletion | CHOLINE-ACETYLTRANSFERASE MUTATIONS | Polymerase chain reaction | Neuromuscular diseases | Usage | Respiratory insufficiency | Gene mutations | Choline | Genetic aspects | Research
Journal Article
Journal of Psychiatric Research, ISSN 0022-3956, 2011, Volume 45, Issue 9, pp. 1250 - 1256
Abstract Linkage studies point to the long arm of chromosome 10 being a susceptibility region for Alzheimer’s disease (AD). Additionally, the gene choline... 
Psychiatry | Depression | Choline acetyltransferase | Alzheimer’s disease | Haplotype | Dementia | Polymorphism
Journal Article
Science, ISSN 0036-8075, 10/2011, Volume 334, Issue 6052, pp. 98 - 101
Journal Article
Neuron, ISSN 0896-6273, 2011, Volume 72, Issue 5, pp. 721 - 733
Journal Article