Related content

A missense mutation c.G2747A (p.R916Q) of gene in dyschromatosis symmetrica hereditaria is not a novel mutation

By Hayashi Masahiro   Suzuki Tamio  

Archives of Dermatological Research, Vol. 302, Iss. 6, 2010-08 ,pp. : 481-482

Springer Publishing Company

Access to resources Recommend Favorite

A novel P gene missense mutation in a Japanese patient with oculocutaneous albinism type II (OCA2)

By Kato A.   Fukai K.   Oiso N.   Hosomi N.   Saitoh S.   Wada T.   Shimizu H.   Ishii M.  

Journal of Dermatological Science, Vol. 31, Iss. 3, 2003-05 ,pp. : 189-192

Elsevier

Access to resources Recommend Favorite

A novel missense mutation in DSRAD in a family with dyschromatosis symmetrica hereditaria

By Li Ming   Yang Li-Jia   Shi Yi-Xin   Huang Hong-Yu  

Archives of Dermatological Research, Vol. 299, Iss. 5-6, 2007-08 ,pp. : 273-275

Springer Publishing Company

Access to resources Recommend Favorite

A novel KIT missense mutation in one Chinese family with piebaldism

By Yin Xian-Yong  

Archives of Dermatological Research, Vol. 301, Iss. 5, 2009-06 ,pp. : 387-389

Springer Publishing Company

Access to resources Recommend Favorite

Characterization of a Novel Point Mutation (Arg432His) in X-Linked Ichthyosis

By Valdes-Flores M.   Jimenez Vaca A.L.   Kofman-Alfaro S.H.   Cuevas-Covarrubias S.A.  

Acta Dermato-Venereologica, Vol. 81, Iss. 1, 2001-01 ,pp. : 54-55

Medical Journals Limited

Access to resources Recommend Favorite