Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and LAMA2[original query] |
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Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years.
G3 (Bethesda, Md.) 2014 Feb 4 (2): 307-14. Shaffer John R, Polk Deborah E, Wang Xiaojing, Feingold Eleanor, Weeks Daniel E, Lee Myoung-Keun, Cuenco Karen T, Weyant Robert J, Crout Richard J, McNeil Daniel W, Marazita Mary |
| Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes. JIMD reports 2015 23 91-100. Komulainen Tuomas, Hautakangas Milla-Riikka, Hinttala Reetta, Pakanen Salla, Vähäsarja Vesa, Lehenkari Petri, Olsen Päivi, Vieira Päivi, Saarenpää-Heikkilä Outi, Palmio Johanna, Tuominen Hannu, Kinnunen Pietari, Majamaa Kari, Rantala Heikki, Uusimaa Johan |
| Copy number variations in a population-based study of Charcot-Marie-Tooth disease. BioMed research international 2015 2015 960404. Høyer Helle, Braathen Geir J, Eek Anette K, Nordang Gry B N, Skjelbred Camilla F, Russell Michael |
| LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies. Muscle & nerve 2015 Oct 52 (4): 547-53. Løkken Nicoline, Born Alfred Peter, Duno Morten, Vissing Jo |
| Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort. Orphanet journal of rare diseases 2021 7 16 (1): 319. Tan Dandan, Ge Lin, Fan Yanbin, Chang Xingzhi, Wang Shuang, Wei Cuijie, Ding Juan, Liu Aijie, Wang Shuo, Li Xueying, Gao Kai, Yang Haipo, Que Chengli, Huang Zhen, Li Chunde, Zhu Ying, Mao Bing, Jin Bo, Hua Ying, Zhang Xiaoli, Zhang Bingbing, Zhu Wenhua, Zhang Cheng, Wang Yanjuan, Yuan Yun, Jiang Yuwu, Rutkowski Anne, Bönnemann Carsten G, Wu Xiru, Xiong H |
| Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes. PeerJ 2021 2 9 e10711. Guelly Christian, Abilova Zhannur, Nuralinov Omirbek, Panzitt Katrin, Akhmetova Ainur, Rakhimova Saule, Kozhamkulov Ulan, Kairov Ulykbek, Molkenov Askhat, Seisenova Ainur, Trajanoski Slave, Abildinova Rashbayeva Gulzhaina, Kaussova Galina, Windpassinger Christian, Lee Joseph H, Zhumadilov Zhaxybay, Bekbossynova Makhabbat, Akilzhanova Ain |
| Hypoglycemia in Patients With LAMA2-CMD. Pediatric neurology 2023 3 143 1-5. Camelo Clara Gontijo, Martins Moreno Cristiane de Araújo, Artilheiro Mariana Cunha, Serafim Silva André Macedo, Quadros Monteiro Fonseca Alulin Tácio, Mendonça de Holanda Rodrigo, Reed Umbertina Conti, Zanoteli Edm |
| Phenotype-genotype spectrum of a cohort of congenital muscular dystrophies: a single-centre experience from India. Neurogenetics 2024 8 . Tanushree Chawla, Saraswati Nashi, Dipti Baskar, Kiran Polavarapu, Seena Vengalil, Mainak Bardhan, Veeramani Preethish-Kumar, Ramya Sukrutha, Gopikrishnan Unnikrishnan, Akshata Huddar, Hansashree Padmanabha, Ram Murthy Anjanappa, Nandeesh Bevinahalli, Vidya Nittur, Manoj Rajanna, Gautham Arunachal Udupi, Atchayaram Nali |
| MYLK*FLNB and DOCK1*LAMA2 gene-gene interactions associated with rheumatoid arthritis in the focal adhesion pathway. Frontiers in genetics 2024 5 15 1375036. Maëva Veyssiere, Maria Del Pilar Rodriguez Ordonez, Smahane Chalabi, Laetitia Michou, François Cornelis, Anne Boland, Robert Olaso, Jean-François Deleuze, Elisabeth Petit-Teixeira, Valérie Chaud |
- Page last reviewed:Feb 1, 2024
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