Inborn errors of metabolism in Latin America: challenges and opportunities
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-010-9112-8
Reference9 articles.
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2. Chamoles NA, Blanco M, Gaggioli D (2001) Diagnosis of alpha-L-iduronidase deficiency in dried blood spots on filter paper: the possibility of newborn diagnosis. Clin Chem 47(4):780–1
3. Giugliani R, Matte U (2004) The Latin American Network of Human Genetics. Comm Genet 7:74–75
4. Kremer RD, Boldini CD, Capra AP, Levstein IM, Bainttein N, Hidalgo PK, Hilba H (1985) Sandhoff disease: 36 cases from Cordoba, Argentina. J Inherit Metab Dis 8(1):46
5. Mathers CD, Loncar D (2006) Projections of global mortality and burden of disease from 2002 to 2030. PLoS Med 3(11):e442
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