首页 > 《国际皮肤性病学杂志（英文）》 > 2020年01期 > Lipoid Proteinosis Due to Homozygous Deletion Mutation (c.735delTG) in the ECM1 Gene Presents with Seizures and Hoarseness but No Skin Involvement

Lipoid Proteinosis Due to Homozygous Deletion Mutation (c.735delTG) in the ECM1 Gene Presents with Seizures and Hoarseness but No Skin Involvement

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DOI ojne9m5mjr/4751561

作者 Vahidnezhad Hassan Youssefian Leila Tafakhori Abbas Li Qiaoli Uitto Jouni Rajabpour Fatemeh Vand Pishnamazi Morteza Modabbernia Amirhossein Tabrizi Mina

机构地区 Molecular Medicine Division, Biotechnology Research Center, Pasteur Institute of Iran, Tehran 14167, Iran;Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran 14167, Iran;Department of Dermatology and Cutaneous Biology, Thomas Jefferson University, Philad

出处《国际皮肤性病学杂志（英文）》 2020年01期

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分类 [医药卫生][]

出版日期 2020年08月13日（中国期刊网平台首次上网日期，不代表论文的发表时间）

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国际皮肤性病学杂志（英文）

国际皮肤性病学杂志（英文）

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