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Correction: Genomic variations of the mevalonate pathway in porokeratosis.

作者信息

Zhang Zhenghua, Li Caihua, Wu Fei, Ma Ruixiao, Luan Jing, Yang Feng, Liu Weida, Wang Li, Zhang Shoumin, Liu Yan, Gu Jun, Hua Wenlian, Fan Min, Peng Hua, Meng Xuemei, Song Ningjing, Bi Xinling, Gu Chaoying, Zhang Zhen, Huang Qiong, Chen Lianjun, Xiang Leihong, Xu Jinhua, Zheng Zhizhong, Jiang Zhengwen

出版信息

Elife. 2016 Jan 27;5:e14383. doi: 10.7554/eLife.14383.

DOI:10.7554/eLife.14383
PMID:26816331
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4744201/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/0a4abd275c56/elife-14383-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/e13ca3bfa8ae/elife-14383-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/381b749b3a61/elife-14383-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/b66bace24b10/elife-14383-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/0a4abd275c56/elife-14383-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/e13ca3bfa8ae/elife-14383-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/381b749b3a61/elife-14383-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/b66bace24b10/elife-14383-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1e7/4744201/0a4abd275c56/elife-14383-fig4.jpg

相似文献

1
Correction: Genomic variations of the mevalonate pathway in porokeratosis.更正：汗孔角化症中甲羟戊酸途径的基因组变异。
Elife. 2016 Jan 27;5:e14383. doi: 10.7554/eLife.14383.
2
Genomic variations of the mevalonate pathway in porokeratosis.汗孔角化症中甲羟戊酸途径的基因组变异
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Arch Dermatol Res. 2014 Oct;306(8):749-55. doi: 10.1007/s00403-014-1465-7. Epub 2014 Apr 30.
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Two closely linked variations in actin cytoskeleton pathway in a Chinese pedigree with disseminated superficial actinic porokeratosis.一个中国播散性浅表性光化性汗孔角化症家系中肌动蛋白细胞骨架途径的两个紧密连锁变异。
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Disseminated superficial actinic porokeratosis.播散性浅表性光化性汗孔角化症
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Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1.12号染色体q23.2-24.1区域弥漫性浅表性光化性汗孔角化症位点的鉴定。
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Australas J Dermatol. 2012 May;53(2):e30-1. doi: 10.1111/j.1440-0960.2011.00787.x. Epub 2011 Jun 23.
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引用本文的文献

1
Establishment of a Mouse Model for Porokeratosis Due to Mevalonate Diphosphate Decarboxylase Deficiency.建立 Mevalonate Diphosphate Decarboxylase 缺陷导致的掌跖角化病小鼠模型。
Skin Res Technol. 2024 Sep;30(9):e70076. doi: 10.1111/srt.70076.
2
Two Cases of Porokeratosis with MVD Mutations, in Association with Bullous Pemphigoid.两例伴有MVD突变的汗孔角化症，与大疱性类天疱疮相关。
Acta Derm Venereol. 2021 Mar 31;101(3):adv00423. doi: 10.2340/00015555-3764.
3
Dermoscopic Features and Gene Mutation in the Mevalonate Pathway of Five Sporadic Patients with Porokeratosis.
5例散发型汗孔角化症患者的皮肤镜特征及甲羟戊酸途径中的基因突变
Chin Med J (Engl). 2017 Jul 20;130(14):1747-1748. doi: 10.4103/0366-6999.209905.