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W. A. Paznekas, S. A. Boyadjiev, R. E. Shapiro, O. Daniels, B. Wollnik, C. E. Keegan, J. W. Innis, M. B. Dinulos, C. Christian, M. C. Hannibal and E. W. Jabs, “Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia,” The American Journal of Human Genetics, Vol. 72, No. 2, 2003, pp. 408-418. doi:10.1086/346090

has been cited by the following article:

• TITLE: Mutations with Hair Shape Phenotypes Abnormalities—The Morphogenetic Waves and Related Diseases

  AUTHORS: Junmin Wang, Guannan Wang, Jintao Zhang

  KEYWORDS: Waved Hair; Curly Hair; Gene Mutations; Diseases

  JOURNAL NAME: Journal of Cosmetics, Dermatological Sciences and Applications, Vol.3 No.3A, August 15, 2013

  ABSTRACT: Hair morphology is one of the most conspicuous features of human variation. The hair follicle has attracted significant attention as a model for the investigation of diverse biological problems. Whereas, very little is known about the genes influencing the morphology and structure of the hair shaft. Curly hair is very common character of hair phenotypes of human, while most congenital curl occurs owing to genetic factors and some are closely related with genetic diseases. This review highlights current related genes reported affecting hair curliness and human diseases which are due to gene mutations.