| [1] | 
													
														FENG Xiaoyan, LU Xinxin, BI Tiantian, LI Qinfeng. 
														
															Keratitis ichthyosis deafness syndrome caused by GJB2 gene mutation
														[J]. China Journal of Leprosy and Skin Diseases, 2023, 39(6): 423-425.
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													| [2] | 
													
														MIAO Mengyu, WANG Zhenzhen, SUN Lele, LIU Hong, ZHANG Furen. 
														
															One novel mutation of the NCSTN gene in one acne inversa family
														[J]. China Journal of Leprosy and Skin Diseases, 2021, 37(8): 486-489.
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													| [3] | 
													
														MA Panpan, ZHANG Chuan, WANG Xing, LIU Furong, HAO Shengju, ZHANG Qinghua, CHEN Xue, ZHOU Bingbo, SUN Qingmei. 
														
															Detection of NF1 gene mutation in three patients with neurofibromatosis type 1
														[J]. China Journal of Leprosy and Skin Diseases, 2021, 37(4): 204-207.
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													| [4] | 
													
														SHOU Xinyi, GU Weizhong, ZHU Kun, LI Yunling. 
														
															Giant juvenile xanthogranuloma on the right auricle: a case report
														[J]. China Journal of Leprosy and Skin Diseases, 2021, 37(1): 32-34.
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													| [5] | 
													
														LIU Lian, ZHANG Zihui, HAO Dan, MEI Rong, LI Erlong, SUN Bensen, JIANG Xian. 
														
															Advances in the Pathogenesis of Port Wine Stains
														[J]. China Journal of Leprosy and Skin Diseases, 2019, 35(4): 253-256.
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													| [6] | 
													
														GUO Yunyi, ZHU Ying, ZHANG Danlu, GUO Birong, SUN Zhonghui. 
														
															Mutations detection in two families with epidermolytic palmoplantar keratoderma
														[J]. China Journal of Leprosy and Skin Diseases, 2019, 35(12): 727-730.
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													| [7] | 
													
														FU Fanghui, FU Xi'an, WANG Zhenzhen, YU Gongqi, LIU Hong, ZHANG Furen. 
														
															Associationof IL36RN mutation with palmoplantar pustulosis
														[J]. China Journal of Leprosy and Skin Diseases, 2019, 35(1): 6-8.
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													| [8] | 
													
														LANG Xiaoqiao, SUN Yonghu, FU Xi'an, SUN Lele, LIU Hong, ZHANG Furen . 
														
															Mutation analysis in three cases with sporadic neurofibromatosis type 1
														[J]. China Journal of Leprosy and Skin Diseases, 2019, 35(1): 9-12.
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													| [9] | 
													
														JI Jin, GUO Qin, ZHANG Ruohua, LI Ming. 
														
															Identification of ADAR1 gene mutation in one sporadic case with dyschromatosis symmetrica hereditaria
														[J]. China Journal of Leprosy and Skin Diseases, 2018, 34(6): 321-323.
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													| [10] | 
													
														LI Lulu, YOU Jiabao, FU Xian, YU Gongqi, LIU Hong, ZHANG Furen, . 
														
															Association of AP1S3 mutation with generalized pustular psoriasis
														[J]. China Journal of Leprosy and Skin Diseases, 2018, 34(3): 131-134.
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													| [11] | 
													
														ZENG Rong, LIU Yuzhen, TONG Jianbo, HE Yanyan, LIN Tong, XU Haoxiang, LI Min.. 
														
															Identification of a novel mutation of ADAR1 gene in a family with dyschromatosis symmetrical hereditaria
														[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(9): 517-519.
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													| [12] | 
													
														ZENG Rong, HE Yanyan, HUI Yun, LI Zhiliang, XU Haoxiang, LI Min.. 
														
															Identification of a novel mutation of KRT9 gene in a family with epidermolytic palmoplantar keratoderma
														[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(8): 465-467.
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													| [13] | 
													
														CHEN Fuying, LI Ming.. 
														
															Update of the abnormal cholesterol metabolism and keratinization genodermatosis
														[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(8): 506-509.
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													| [14] | 
													
														CHEN Pingjiao, LI Changxing, ZENG Kang, ZHANG Xibao.. 
														
															Update of the genetics of bullous congenital ichthyosiform erythroderma
														[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(6): 381-384.
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													| [15] | 
													
														CAO Jing, SUN Lele, FU Xian, WANG Zhenzhen, YU Gongqi, LIU Hong, ZHANG Furen. 
														
															Detection of KTR gene mutations in a family with pachyonychia congenital type II
														[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(2): 70-73.
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