Marked intrafamilial phenotypic heterogeneity in dystrophic epidermolysis bullosa caused by inheritance of a mild dominant glycine substitution and a novel deep intronic recessiveCOL7A1mutation

MLA

Sandrina Turczynski, et al. “Marked Intrafamilial Phenotypic Heterogeneity in Dystrophic Epidermolysis Bullosa Caused by Inheritance of a Mild Dominant Glycine Substitution and a Novel Deep Intronic RecessiveCOL7A1mutation.” British Journal of Dermatology, vol. 174, Feb. 2016, pp. 1122–25. EBSCOhost, https://doi.org/10.1111/bjd.14312.

APA

Sandrina Turczynski, Dedee F. Murrell, Matthias Titeux, H.I. Cohn, Alain Hovnanian, & N. Pironon. (2016). Marked intrafamilial phenotypic heterogeneity in dystrophic epidermolysis bullosa caused by inheritance of a mild dominant glycine substitution and a novel deep intronic recessiveCOL7A1mutation. British Journal of Dermatology, 174, 1122–1125. https://doi.org/10.1111/bjd.14312

Chicago

Sandrina Turczynski, Dedee F. Murrell, Matthias Titeux, H.I. Cohn, Alain Hovnanian, and N. Pironon. 2016. “Marked Intrafamilial Phenotypic Heterogeneity in Dystrophic Epidermolysis Bullosa Caused by Inheritance of a Mild Dominant Glycine Substitution and a Novel Deep Intronic RecessiveCOL7A1mutation.” British Journal of Dermatology 174 (February): 1122–25. doi:10.1111/bjd.14312.