Similar articles for PMID: 24498303

Year	Number of Results
1997	1
2002	1
2003	1
2004	3
2005	3
2006	2
2007	3
2008	3
2009	2
2010	6
2011	6
2012	13
2013	19
2014	20
2015	10
2016	12
2017	15
2018	10
2019	15
2020	11
2021	13
2022	6
2023	5
2024	0

1

Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.

Liu H, Li Y, Hung KK, Wang N, Wang C, Chen X, Sheng D, Fu X, See K, Foo JN, Low H, Liany H, Irwan ID, Liu J, Yang B, Chen M, Yu Y, Yu G, Niu G, You J, Zhou Y, Ma S, Wang T, Yan X, Goh BK, Common JE, Lane BE, Sun Y, Zhou G, Lu X, Wang Z, Tian H, Cao Y, Chen S, Liu Q, Liu J, Zhang F. Liu H, et al. PLoS One. 2014 Feb 3;9(2):e87250. doi: 10.1371/journal.pone.0087250. eCollection 2014. PLoS One. 2014. PMID: 24498303 Free PMC article.

2

Mutations in ABCB6 cause dyschromatosis universalis hereditaria.

Zhang C, Li D, Zhang J, Chen X, Huang M, Archacki S, Tian Y, Ren W, Mei A, Zhang Q, Fang M, Su Z, Yin Y, Liu D, Chen Y, Cui X, Li C, Yang H, Wang Q, Wang J, Liu M, Deng Y. Zhang C, et al. J Invest Dermatol. 2013 Sep;133(9):2221-8. doi: 10.1038/jid.2013.145. Epub 2013 Mar 21. J Invest Dermatol. 2013. PMID: 23519333 Free article.

3

Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria.

Cui YX, Xia XY, Zhou Y, Gao L, Shang XJ, Ni T, Wang WP, Fan XB, Yin HL, Jiang SJ, Yao B, Hu YA, Wang G, Li XJ. Cui YX, et al. PLoS One. 2013 Nov 5;8(11):e79808. doi: 10.1371/journal.pone.0079808. eCollection 2013. PLoS One. 2013. PMID: 24224009 Free PMC article.

4

Novel missense mutation of SASH1 in a Chinese family with dyschromatosis universalis hereditaria.

Cao L, Zhang R, Yong L, Chen S, Zhang H, Chen W, Xu Q, Ge H, Mao Y, Zhen Q, Yu Y, Hu X, Sun L. Cao L, et al. BMC Med Genomics. 2021 Jun 26;14(1):168. doi: 10.1186/s12920-021-01014-w. BMC Med Genomics. 2021. PMID: 34174894 Free PMC article.

5

Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria.

Lu C, Liu J, Liu F, Liu Y, Ma D, Zhang X. Lu C, et al. J Dermatol Sci. 2014 Dec;76(3):255-8. doi: 10.1016/j.jdermsci.2014.08.015. Epub 2014 Sep 11. J Dermatol Sci. 2014. PMID: 25288164 No abstract available.

6

Two novel SASH1 mutations in Chinese families with dyschromatosis universalis hereditaria.

Liu JW, Habulieti X, Wang RR, Ma DL, Zhang X. Liu JW, et al. J Clin Lab Anal. 2021 Jun;35(6):e23803. doi: 10.1002/jcla.23803. Epub 2021 May 24. J Clin Lab Anal. 2021. PMID: 34028087 Free PMC article.

7

The PER3^rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria.

Chen H, Yang P, Yang D, Wang D, Lu M, Li Y, Zhong Z, Zhang J, Zeng Z, Liu Z, Zeng X, Jia X, Xing Q, Zhou D. Chen H, et al. J Mol Med (Berl). 2023 Mar;101(3):279-294. doi: 10.1007/s00109-023-02288-6. Epub 2023 Feb 15. J Mol Med (Berl). 2023. PMID: 36790533

8

Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing.

Liu JW; Asan; Sun J, Vano-Galvan S, Liu FX, Wei XX, Ma DL. Liu JW, et al. Chin Med J (Engl). 2016 Jan 5;129(1):33-8. doi: 10.4103/0366-6999.172564. Chin Med J (Engl). 2016. PMID: 26712430 Free PMC article.

9

Atypical presentation of dyschromatosis universalis hereditaria with a novel ABCB6 mutation.

Zhong W, Pan Y, Shao Y, Yang Y, Yu B, Lin Z. Zhong W, et al. Clin Exp Dermatol. 2019 Apr;44(3):e58-e60. doi: 10.1111/ced.13833. Epub 2018 Nov 14. Clin Exp Dermatol. 2019. PMID: 30430618 No abstract available.

10

Identification of a Novel Mutation in SASH1 Gene in a Chinese Family With Dyschromatosis Universalis Hereditaria and Genotype-Phenotype Correlation Analysis.

Wu N, Tang L, Li X, Dai Y, Zheng X, Gao M, Wang P. Wu N, et al. Front Genet. 2020 Aug 4;11:841. doi: 10.3389/fgene.2020.00841. eCollection 2020. Front Genet. 2020. PMID: 32849825 Free PMC article.

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