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Autor:
Arzu Selamioğlu, Zelal Tandoğan, Mehmet Cihan Balcı, Meryem Karaca, Tuğba Kozanoğlu, Alihan Yesil, Gülden Gökçay
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101154- (2024)
Phenylketonuria (PKU) results from a deficiency in phenylalanine hydroxylase, catalyzing the conversion of phenylalanine (Phe) to tyrosine. Premenstrual syndrome (PMS) consists of physical, behavioral, and emotional symptoms occurring during the last
Externí odkaz:
https://doaj.org/article/3919ada5d5314c5db1b701f315bad64e
