Phenotypic and mutational spectrum of thirty-five patients with Sjogren-Larsson syndrome: identification of eleven novel ALDH3A2 mutations and founder effects

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作者： Abdel-Hamid, Mohamed S. ^[1] ; Issa, Mahmoud Y. ^[2] ; Elbendary, Hasnaa M. ^[3] ; Abdel-Ghafar, Sherif F. ^[4] ; Rafaat, Karima ; Hosny, Heba ; Girgis, Marian ; Abdel-Salam, Ghada M. H. ; Zaki, Maha S.

作者单位： Natl Res Ctr, Clin Genet Dept, Human Genet & Genome Res Div, Cairo, Egypt ^[1] Cairo Univ, Fac Med, Pediat Dept, Cairo, Egypt ^[2] Natl Res Ctr, Med Mol Genet Dept, Human Genet & Genome Res Div, Cairo, Egypt ^[3] Natl Inst Neuromotor Syst, Cairo, Egypt ^[4]

发布时间 2020-02-11

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Journal of human genetics

2019年64卷9期

859-865页

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Phenotypic and mutational spectrum of thirty-five patients with Sjogren-Larsson syndrome: identification of eleven novel ALDH3A2 mutations and founder effects

Journal of human genetics

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Journal of human genetics

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Phenotypic and mutational spectrum of thirty-five patients with Sjogren-Larsson syndrome: identification of eleven novel ALDH3A2 mutations and founder effects

Journal of human genetics

相似文献

Journal of human genetics

相关期刊

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