Homozygous Missense Mutation in the ECM1 Gene in Chinese Siblings with Lipoid Proteinosis

By Han Beibei   Zhang Xinglian   Liu Qiang   Chen Xixue   Zhu Xuejun  

Acta Dermato-Venereologica, Vol. 87, Iss. 5, 2007-09 ,pp. : 387-389

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Lipoid Proteinosis Resulting from a Large Homozygous Deletion Affecting Part of the ECM1 Gene and Adjacent Long Non-coding RNA

By Lee Ming-Yang   Wang– Hui-Jun   Han Ying   Zhou Yun   Zhao Jia-Hui   Duo– Li-Na   Feng Cheng   Hua Hong   Liu Hong-Wei   Lin Zhi-Miao   Yang Yong  

Acta Dermato-Venereologica, Vol. 95, Iss. 5, 2015-05 ,pp. : 608-610

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Novel and Recurrent FERMT1 Gene Mutations in Kindler Syndrome

By Techanukul Tanasit   Sethuraman Gomathy   Zlotogorski Abraham   Horev Liran   Macarov Michal   Trainer Alison   Fong Kenneth   Lens Marko   Medenica Ljiljana   Ramesh Venkatesh   McGrath John A.   Lai-Cheong Joey E.  

Acta Dermato-Venereologica, Vol. 91, Iss. 3, 2011-05 ,pp. : 267-270

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Genotype–Phenotype Correlations in a Prospective Cohort Study of Paediatric Plaque Psoriasis: Lack of Correlation Between HLA-C*06 and Family History of Psoriasis

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Acta Dermato-Venereologica, Vol. 94, Iss. 6, 2014-11 ,pp. : 667-671

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Novel and Recurrent KIND1 Mutations in Two Patients with Kindler Syndrome and Severe Mucosal Involvement

By Mansur Tülin A.   Elcioglu Nursel H.   Aydıngöz Ikbal E.   Akkaya Deniz A.   Serdar Zehra Asiran   Herz Corinna   Bruckner-Tuderman Leena   Has Cristina  

Acta Dermato-Venereologica, Vol. 87, Iss. 6, 2007-10 ,pp. : 563-565

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