Progressive symmetric erythrokeratodermia with spinocerebellar ataxia due to ELOVL4 mutation in a Chinese family

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dc.contributor.authorWang, Zijuanen_US
dc.contributor.authorLin, Zhimiaoen_US
dc.contributor.authorWang, Huijunen_US
dc.date.accessioned2023-08-10T07:29:32Z
dc.date.available2023-08-10T07:29:32Z
dc.date.issued2022-02
dc.identifier.affiliationsDepartment of Dermatology, Peking University First Hospital, Beijing Key Laboratory of Molecular Diagnosis on Dermatoses, National Clinical Research Center for Skin and Immune Diseases, Beijing, ChinaHuijunen_US
dc.identifier.citationWang, Zijuanen_US
dc.identifier.citationLin, Zhimiaoen_US
dc.identifier.citationWang, Huijun. Progressive symmetric erythrokeratodermia with spinocerebellar ataxia due to ELOVL4 mutation in a Chinese family. Indian Journal of Dermatology, Venereology and Leprology. 2022 Feb; 88(1): 132en_US
dc.identifier.issn0973-3922
dc.identifier.issn0378-6323
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/222908
dc.languageenen_US
dc.publisherScientific Scholaren_US
dc.relation.issuenumber1en_US
dc.relation.volume88en_US
dc.source.urihttps://doi.org/10.25259/IJDVL_488_20en_US
dc.titleProgressive symmetric erythrokeratodermia with spinocerebellar ataxia due to ELOVL4 mutation in a Chinese familyen_US
dc.typeJournal Articleen_US
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