phenylketonuria音标
英 [fenəlki:tə'njʊərɪə]
美 [ˌfenəlˌkitn'jʊrˌfenəlˌkitn'ʊriə]
phenylketonuria翻译
n.
苯丙酮尿,苯丙酮酸尿症(一种先天性代谢异常);
英英释义
phenylketonuria[ 'fenil,ki:tə'njuri:ə, 'fi:- ]
n.a genetic disorder of metabolism; lack of the enzyme needed to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency
同义词:PKU
phenylketonuria用法
权威例句
Phenylketonuria
Phenylketonuria
Phenylketonuria
Monogenic traits are not simple: lessons from phenylketonuria.
Neuropsychology of Early-Treated Phenylketonuria: Specific Executive Function Deficits
Neuropsychology of Early-treated Phenylketonuria: Specific Executive Function Deficits
Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies.
A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.
Cell encapsulation as a potential nondietary therapy for maternal phenylketonuria.
Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome.