Dyschromatosis symmetrica hereditaria in a family with twelve patients

Chinese Journal of Medical Genetics

Volumn 29, Issue 3, 2012, Pages 299-

  Liu, Xiang ^a   Li, Xi Ying ^a   Deng, Wei Ping ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL ARTICLE; DYSCHROMATOSIS SYMMETRICA HEREDITARIA; GENETIC DISORDER; HUMAN; SKIN DISEASE;

EID: 84863434063     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.1003-9406.2012.03.031     Document Type: Article

References (4)

1. Zhu GD. Dyschromatosis symmetrica hereditaria. In: Zhao B ed. China clinical dermatology. 1st ed. Nanjing: Jiangsu Science and Technology Press, 2009,1249-1250.
2. Zhang XJ, Gao M, Li M, et al. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21. J Invest Dermatol, 2003,120:776-780. (Pubitemid 36529077)
3. Shi BJ, Xue M, Liu Y, et al. First report of the coexistence of dyschromatosis symmetrica hereditaria and psoriasis: one novel TCT to A mutation in the double-RNA-specific adenosine deaminase gene. J Eur Acad Dermatol Venereol, 2012,26:657-658.
4. Tojyo K, Hattori T, Sekijima Y, et al. A case of idiopathic brain calcification associated with dyschromatosis symmetrica hereditaria, aplasia of dental root, and aortic valve sclerosis. Rinsho Shinkeigaku, 2001,41:299-305. (Pubitemid 34024110)