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...
| Published in: | مجله دانشگاه علوم پزشکی بیرجند |
|---|---|
| Main Authors: | , |
| Format: | Article |
| Language: | Persian |
| Published: |
Birjand University of Medical Sciences and Health Services
2015-10-01
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| Subjects: | |
| Online Access: | http://journal.bums.ac.ir/browse.php?a_code=A-10-1524-1&slc_lang=en&sid=1 |