Incidence of Phenylketonuria in Southern Khorasan (2012- 2014): Short Communication
Background and Aim: Phenylketonuria (PKU., OMIM261600) is the most common genetic disorder autosomal recessive mode of inheritance and the metabolism of amino-acids, which is due to deficiency of the liver enzyme phenylalanine - hydroxylase as a result of mutations in the gene encoding it is achieve...
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| Principais autores: | , |
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| Format: | Artigo |
| Sprog: | Persa |
| Udgivet: |
Birjand University of Medical Sciences and Health Services
2015-10-01
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| Serier: | مجله دانشگاه علوم پزشکی بیرجند |
| Fag: | |
| Online adgang: | http://journal.bums.ac.ir/browse.php?a_code=A-10-1524-1&slc_lang=en&sid=1 |
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