Novel frameshift mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria

Journal of the European Academy of Dermatology and Venereology

Volumn 22, Issue 11, 2008, Pages 1375-1376

  Ren, J W ^a   Luo, S J ^a   Peng, Z H ^a   Liu, Y ^a   Pan, M ^a   Xiao, S X ^a  

^a XI'AN JIAOTONG UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CHINESE; DSRAD GENE; DYSCHROMATOSIS SYMMETRICA HEREDITARIA; EXON; FRAMESHIFT MUTATION; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; HUMAN; LETTER; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RNA GENE; SKIN DEFECT; SKIN DISEASE; SUN EXPOSURE;

ADULT; CHINA; CHROMOSOME MAPPING; FRAMESHIFT MUTATION; HUMANS; MALE; PIGMENTATION DISORDERS; POLYMERASE CHAIN REACTION;

EID: 53749091948     PISSN: 09269959     EISSN: 14683083     Source Type: Journal    
DOI: 10.1111/j.1468-3083.2008.02632.x     Document Type: Letter

References (6)

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2. He PP, He CD, Cui Y et al. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China. Br J Dermatol 2004 150 : 633 639.
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5. Miyamura Y, Suzuki T, Kono M et al. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am J Hum Genet 2003 73 : 693 699.
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