Methylmalonic acidemia: Current status and research priorities
Author:
Affiliation:
1. Shandong Academy of Medical Science, Shandong Medical Biotechnological Center, Key Laboratory for Biotech Drugs of the Ministry of Health
Publisher
International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/irdr/7/2/7_2018.01026/_pdf
Reference30 articles.
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2. 2. Liu J, Peng Y, Zhou N, Liu X, Meng Q, Xu H, Zhao S. Combined methylmalonic acidemia and homocysteinemia presenting predominantly with late-onset diffuse lung disease: A case series of four patients. Orphanet J Rare Dis. 2017; 12:58.
3. 3. Matsui SM, Mahoney MJ, Rosenberg LE. The natural history of the inherited acidemias. N Engl J Med. 1983; 308:857-861.
4. 4. Harrington EA, Sloan JL, Manoli I, Chandler RJ, Schneider M, McGuire PJ, Calcedo R, Wilson JM, Venditti CP. Neutralizing Antibodies Against Adeno-Associated Viral Capsids in Patients with mut Methylmalonic Acidemia. Hum Gene Ther. 2016; 27:345-353.
5. 5. Qiliang L, Wenqi S, Quan W, Xinying Y, Jiuwei L, Qiang S, Xiaoxia P, Peichang W. Predictors of survival in children with methymalonic acidemia with homocystinuria in Beijing, China: A prospective cohort study. Indian Pediatr. 2015; 52:119-124.
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