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Autor:
Oliveira, Nalyne Carvalho de, Rosa, Camilla Karinne Guimarães, Cartaxo, Émile Dantas de Carvalho, Rosa, David de Melo Arimatea, Oliveira, Halley Ferraro
Publikováno v:
Research, Society and Development; Vol. 11 No. 4; e5911427026
Research, Society and Development; Vol. 11 Núm. 4; e5911427026
Research, Society and Development; v. 11 n. 4; e5911427026
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 11 Núm. 4; e5911427026
Research, Society and Development; v. 11 n. 4; e5911427026
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Phenylketonuria (PKU) is a genetic disease, of autosomal recessive inheritance, caused by biallelic mutations in the PAH gene that encodes the enzyme phenylalanine hydroxylase (FAH) whose treatment is only dietary (BRASIL, 2019). The available litera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::255c025876ddc55342db7ee8a298c418
https://rsdjournal.org/index.php/rsd/article/view/27026
https://rsdjournal.org/index.php/rsd/article/view/27026