These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
165 related articles for article (PubMed ID: 26080897)
1. Choline Acetyltransferase Mutations Causing Congenital Myasthenic Syndrome: Molecular Findings and Genotype-Phenotype Correlations. Arredondo J; Lara M; Gospe SM; Mazia CG; Vaccarezza M; Garcia-Erro M; Bowe CM; Chang CH; Mezei MM; Maselli RA Hum Mutat; 2015 Sep; 36(9):881-93. PubMed ID: 26080897 [TBL] [Abstract][Full Text] [Related]
2. Functional consequences and structural interpretation of mutations of human choline acetyltransferase. Shen XM; Crawford TO; Brengman J; Acsadi G; Iannaconne S; Karaca E; Khoury C; Mah JK; Edvardson S; Bajzer Z; Rodgers D; Engel AG Hum Mutat; 2011 Nov; 32(11):1259-67. PubMed ID: 21786365 [TBL] [Abstract][Full Text] [Related]
3. Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans. Ohno K; Tsujino A; Brengman JM; Harper CM; Bajzer Z; Udd B; Beyring R; Robb S; Kirkham FJ; Engel AG Proc Natl Acad Sci U S A; 2001 Feb; 98(4):2017-22. PubMed ID: 11172068 [TBL] [Abstract][Full Text] [Related]
4. Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesis. Maselli RA; Chen D; Mo D; Bowe C; Fenton G; Wollmann RL Muscle Nerve; 2003 Feb; 27(2):180-7. PubMed ID: 12548525 [TBL] [Abstract][Full Text] [Related]
5. Clinical and Genetic Features of Congenital Myasthenic Syndromes due to CHAT Mutations: Case Report and Literature Review. Arican P; Gencpinar P; Cavusoglu D; Olgac Dundar N Neuropediatrics; 2018 Aug; 49(4):283-288. PubMed ID: 29783273 [TBL] [Abstract][Full Text] [Related]
6. Protein kinase C isoforms differentially phosphorylate human choline acetyltransferase regulating its catalytic activity. Dobransky T; Doherty-Kirby A; Kim AR; Brewer D; Lajoie G; Rylett RJ J Biol Chem; 2004 Dec; 279(50):52059-68. PubMed ID: 15381704 [TBL] [Abstract][Full Text] [Related]
7. Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferase. Schmidt C; Abicht A; Krampfl K; Voss W; Stucka R; Mildner G; Petrova S; Schara U; Mortier W; Bufler J; Huebner A; Lochmüller H Neuromuscul Disord; 2003 Mar; 13(3):245-51. PubMed ID: 12609506 [TBL] [Abstract][Full Text] [Related]
8. Congenital myasthenic syndrome with episodic apnea in patients homozygous for a CHAT missense mutation. Kraner S; Laufenberg I; Strassburg HM; Sieb JP; Steinlein OK Arch Neurol; 2003 May; 60(5):761-3. PubMed ID: 12756141 [TBL] [Abstract][Full Text] [Related]
9. Mutation of a serine near the catalytic site of the choline acetyltransferase a gene almost completely abolishes motility of the zebrafish embryo. Joshi S; Virdi S; Etard C; Geisler R; Strähle U PLoS One; 2018; 13(11):e0207747. PubMed ID: 30458023 [TBL] [Abstract][Full Text] [Related]
10. Clinical variability of CMS-EA (congenital myasthenic syndrome with episodic apnea) due to identical CHAT mutations in two infants. Barisic N; Müller JS; Paucic-Kirincic E; Gazdik M; Lah-Tomulic K; Pertl A; Sertic J; Zurak N; Lochmüller H; Abicht A Eur J Paediatr Neurol; 2005; 9(1):7-12. PubMed ID: 15701560 [TBL] [Abstract][Full Text] [Related]
11. A multidimensional computational exploration of congenital myasthenic syndrome causing mutations in human choline acetyltransferase. Janežič M; Dileep KV; Zhang KYJ J Cell Biochem; 2021 Aug; 122(8):787-800. PubMed ID: 33650116 [TBL] [Abstract][Full Text] [Related]
12. How chromosomal deletions can unmask recessive mutations? Deletions in 10q11.2 associated with CHAT or SLC18A3 mutations lead to congenital myasthenic syndrome. Schwartz M; Sternberg D; Whalen S; Afenjar A; Isapof A; Chabrol B; Portnoï MF; Heide S; Keren B; Chantot-Bastaraud S; Siffroi JP Am J Med Genet A; 2018 Jan; 176(1):151-155. PubMed ID: 29130637 [TBL] [Abstract][Full Text] [Related]
13. Choline acetyltransferase structure reveals distribution of mutations that cause motor disorders. Cai Y; Cronin CN; Engel AG; Ohno K; Hersh LB; Rodgers DW EMBO J; 2004 May; 23(10):2047-58. PubMed ID: 15131697 [TBL] [Abstract][Full Text] [Related]
14. Congenital myasthenic syndrome due to novel CHAT mutations in an ethnic kadazandusun family. Tan JS; Ambang T; Ahmad-Annuar A; Rajahram GS; Wong KT; Goh KJ Muscle Nerve; 2016 May; 53(5):822-6. PubMed ID: 26789281 [TBL] [Abstract][Full Text] [Related]
15. Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations. Schara U; Christen HJ; Durmus H; Hietala M; Krabetz K; Rodolico C; Schreiber G; Topaloglu H; Talim B; Voss W; Pihko H; Abicht A; Müller JS; Lochmüller H Eur J Paediatr Neurol; 2010 Jul; 14(4):326-33. PubMed ID: 19900826 [TBL] [Abstract][Full Text] [Related]