Author:
Zong Yanan,Liu Ning,Zhao Zhenhua,Kong Xiangdong
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference18 articles.
1. Fowler B, Leonard JV, Baumgartner MR. Causes of and diagnostic approach to methylmalonic acidurias. J Inherit Metab Dis. 2008;31:350–60.
2. Nuria CC, David A, Charles PV: Disorders of intracellular cobalamin metabolism. Gene Reviews[Internet].
3. Carrillo-Carrasco N, Chandler RJ, Venditti CP. Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management. J Inherit Metab Dis. 2012;35:91–102.
4. Carrillo-Carrasco N, Venditti CP. Combined methylmalonic acidemia and homocystinuria, cblC type. II. Complications, pathophysiology, and outcomes. J Inherit Metab Dis. 2012;35:103–14.
5. Liu YP, Ma YY, Wu TF, Wang Q, Li XY, Ding Y, et al. Abnormal findings during newborn period of 160 patients with early-onset methylmalonic aciduria. Zhonghua er ke za zhi Chi J pediatr. 2012;50:410–4.
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