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First Case Report of EX3del4765 Mutation in PAH Gene in Asian Population
INTRODUCTION: Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism, which is caused by mutation in phenylalanine hydroxylase (PAH) gene. Most of the PAH mutations are missense mutations (67%), which are followed by small or large deletions (13%). CASE PRESENTATION...
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| Publicado no: | Iran Red Crescent Med J |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Kowsar
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4862320/ https://ncbi.nlm.nih.gov/pubmed/27175306 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5812/ircmj.21633 |
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