Copy For Citation
Luleyap U., PAZARCI P., CÖMERTPAY G., Onenli H. N., PAZARBAŞI A., ALPTEKİN D., ...More
CUKUROVA MEDICAL JOURNAL, vol.41, no.4, pp.702-708, 2016 (ESCI)
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Publication Type:
Article / Article
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Volume:
41
Issue:
4
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Publication Date:
2016
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Doi Number:
10.17826/cutf.254199
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Journal Name:
CUKUROVA MEDICAL JOURNAL
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Journal Indexes:
Emerging Sources Citation Index (ESCI), TR DİZİN (ULAKBİM)
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Page Numbers:
pp.702-708
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Çukurova University Affiliated:
Yes
Abstract
Purpose: Phenylketonuria is an autosomal recessive deficiency of the hepatic enzyme phenylalanine hydroxylase. With this study, detection of the most frequent phenylalanine hydroxylase gene mutations in Turkish population is aimed.