Newborn Screening for Homocystinuria Revealed a High Frequency of MAT I/III Deficiency in Iberian Peninsula

Acessível em: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375120/

Bibliographic Details
Main Author: Marcão, Ana (author)
Other Authors: Couce, María L. (author), Nogueira, Célia (author), Fonseca, Helena (author), Ferreira, Filipa (author), Fraga, José M. (author), Bóveda, M. Dolores (author), Vilarinho, Laura (author)
Format: article
Language:eng
Published: 2016
Subjects:
Rastreio Neonatal
Homocistinúria
Deficiência em MAT I/III
Doenças Genéticas
Online Access:http://hdl.handle.net/10400.18/3330
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/3330

Internet

http://hdl.handle.net/10400.18/3330

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