Translational Science of Rare Diseases, volume 5, issue 1-2, pages 3-58
Disorders of phenylalanine and tyrosine metabolism
Publication type: Journal Article
Publication date: 2020-07-16
Q3
SJR: 0.515
CiteScore: 2.1
Impact factor: —
ISSN: 22146490, 22146512
General Medicine
Abstract
This article provides a review of the inborn errors of phenylalanine and tyrosine metabolism including the diagnostic approach, dietary and pharmalogical management and emerging therapies. Hyperphenylalaninaemia results mainly from defects in either
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GOST
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Alsharhan H. et al. Disorders of phenylalanine and tyrosine metabolism // Translational Science of Rare Diseases. 2020. Vol. 5. No. 1-2. pp. 3-58.
GOST all authors (up to 50)
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Alsharhan H., Ficicioglu C. Disorders of phenylalanine and tyrosine metabolism // Translational Science of Rare Diseases. 2020. Vol. 5. No. 1-2. pp. 3-58.
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RIS
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TY - JOUR
DO - 10.3233/trd-200049
UR - https://doi.org/10.3233/trd-200049
TI - Disorders of phenylalanine and tyrosine metabolism
T2 - Translational Science of Rare Diseases
AU - Alsharhan, Hind
AU - Ficicioglu, Can
PY - 2020
DA - 2020/07/16
PB - IOS Press
SP - 3-58
IS - 1-2
VL - 5
SN - 2214-6490
SN - 2214-6512
ER -
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BibTex (up to 50 authors)
Copy
@article{2020_Alsharhan,
author = {Hind Alsharhan and Can Ficicioglu},
title = {Disorders of phenylalanine and tyrosine metabolism},
journal = {Translational Science of Rare Diseases},
year = {2020},
volume = {5},
publisher = {IOS Press},
month = {jul},
url = {https://doi.org/10.3233/trd-200049},
number = {1-2},
pages = {3--58},
doi = {10.3233/trd-200049}
}
Cite this
MLA
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Alsharhan, Hind, et al. “Disorders of phenylalanine and tyrosine metabolism.” Translational Science of Rare Diseases, vol. 5, no. 1-2, Jul. 2020, pp. 3-58. https://doi.org/10.3233/trd-200049.