Rare compound heterozygous frameshift mutations in ALMS1 gene identified through exome sequencing in a Taiwanese patient with Alström syndrome

研究成果: Article同行評審

10 引文 斯高帕斯(Scopus)

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深入研究「Rare compound heterozygous frameshift mutations in ALMS1 gene identified through exome sequencing in a Taiwanese patient with Alström syndrome」主題。共同形成了獨特的指紋。

Medicine & Life Sciences