Objective To establish a method with high efficiency in detecting phenylalanine hydroxylase(PAH) gene mutations and hence to rapidly diagnose prenatal fetals with phenylketonuria.
英
美
释义
目的提高苯丙氨酸羟化酶基因突变的检出效率,快速对苯丙酮尿症患儿进行产前诊断。
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