Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management.

Authors

Nuria Carrillo-Carrasco, National Institutes of Health
Randy J. Chandler, George Washington University
Charles P. Venditti, National Institutes of Health

Document Type

Journal Article

Publication Date

1-2012

Journal

Journal of Inherited Metabolic Disease

Volume

Volume 35, Issue 1

Inclusive Pages

91-102

Keywords

Amino Acid Metabolism; Inborn Errors--diagnosis; Amino Acid Metabolism; Inborn Errors--genetics; Carrier Proteins--genetics; Homocystinuria--diagnosis; Homocystinuria--genetics; Vitamin B 12--metabolism

Comments

This is an open access PubMed Central article. Click on link for full-text access.

APA Citation

Carrillo-Carrasco, N., Chandler, R. J., & Venditti, C. P. (2012). Combined methylmalonic acidemia and homocystinuria, cblC type. I. clinical presentations, diagnosis and management. Journal of Inherited Metabolic Disease, 35(1), 91-102.

Peer Reviewed

1

Open Access

1