Homozygous missense mutation in the LIPH gene causing autosomal recessive hypotrichosis simplex in a Chinese patient

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Veröffentlicht in:Journal of dermatology 2014-01, Vol.41 (1), p.105-107
Hauptverfasser: Liu, Linghua H., Wang, Jingwen W., Chen, Gang, Chang, Ruixue X., Zhou, Yi, Tang, Huayang Y., Zhu, Jun, Wang, Peiguang G., Yang, Sen, Zhang, Xuejun J.
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container_title Journal of dermatology
container_volume 41
creator Liu, Linghua H.
Wang, Jingwen W.
Chen, Gang
Chang, Ruixue X.
Zhou, Yi
Tang, Huayang Y.
Zhu, Jun
Wang, Peiguang G.
Yang, Sen
Zhang, Xuejun J.
description
doi_str_mv 10.1111/1346-8138.12309
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subjects Alopecia - congenital
Alopecia - genetics
Asian Continental Ancestry Group
Child
China
Homozygote
Humans
Hypotrichosis - congenital
Hypotrichosis - genetics
Lipase - genetics
Male
Mutation, Missense
Scalp - abnormalities
title Homozygous missense mutation in the LIPH gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
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