Author:
Yu Hung-Chun,Sloan Jennifer L.,Scharer Gunter,Brebner Alison,Quintana Anita M.,Achilly Nathan P.,Manoli Irini,Coughlin Curtis R.,Geiger Elizabeth A.,Schneck Una,Watkins David,Suormala Terttu,Van Hove Johan L.K.,Fowler Brian,Baumgartner Matthias R.,Rosenblatt David S.,Venditti Charles P.,Shaikh Tamim H.
Subject
Genetics(clinical),Genetics
Reference36 articles.
1. Inborn errors of cobalamin absorption and metabolism;Watkins;Am. J. Med. Genet. C. Semin. Med. Genet.,2011
2. Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations;Lerner-Ellis;Hum. Mutat.,2009
3. Cobalamin C defect: natural history, pathophysiology, and treatment;Martinelli;J. Inherit. Metab. Dis.,2011
4. Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management;Carrillo-Carrasco;J. Inherit. Metab. Dis.,2012
5. Combined methylmalonic acidemia and homocystinuria, cblC type. II. Complications, pathophysiology, and outcomes;Carrillo-Carrasco;J. Inherit. Metab. Dis.,2012
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