APA

Gostyńska K. B., Nijenhuis M., Lemmink H., Pas H. H., Pasmooij A. M. G., Lang K. K., Castañón M. J., Wiche G. & Jonkman M. F. (20160216). Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex. : Human molecular genetics.

Chicago

Gostyńska Katarzyna B, Nijenhuis Miranda, Lemmink Henny, Pas Hendri H, Pasmooij Anna M G, Lang Kristin Kernland, Castañón Maria J, Wiche Gerhard and Jonkman Marcel F. 20160216. Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex. : Human molecular genetics.

Harvard

Gostyńska K. B., Nijenhuis M., Lemmink H., Pas H. H., Pasmooij A. M. G., Lang K. K., Castañón M. J., Wiche G. and Jonkman M. F. (20160216). Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex. : Human molecular genetics.

MLA

Gostyńska Katarzyna B, Nijenhuis Miranda, Lemmink Henny, Pas Hendri H, Pasmooij Anna M G, Lang Kristin Kernland, Castañón Maria J, Wiche Gerhard and Jonkman Marcel F. Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex. : Human molecular genetics. 20160216.