Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria-Reference-Cited by-同舟云学术

Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria

Published:2013-09 Issue:9 Volume:133 Page:2221-2228
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Zhang Caie,Li Duanzhuo,Zhang Jianguo,Chen Xingping,Huang Mi,Archacki Stephen,Tian Yuke,Ren Weiping,Mei Aihua,Zhang Qingyan,Fang Mingyan,Su Zheng,Yin Ye,Liu Dongxian,Chen Yingling,Cui Xiukun,Li Chang,Yang Huanming,Wang Qing,Wang Jun,Liu Mugen,Deng Yunhua

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference26 articles.

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3. Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification;Dai;Am J Med Genet B Neuropsychiatr Genet,2010

4. Dyschromatosis universalis hereditaria: report of a case and review of the literature;Hawsawi;Pediatr Dermatol,2002

5. ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis;Helias;Nat Genet,2012

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