Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer

MLA

Antonella Verrienti, et al. “Whole Exome Sequencing Identifies a Germline MET Mutation in Two Siblings with Hereditary Wild-Type RET Medullary Thyroid Cancer.” Human Mutation, vol. 39, Dec. 2017, pp. 371–77. EBSCOhost, https://doi.org/10.1002/humu.23378.

APA

Antonella Verrienti, Ferdinando Marandino, Diego Russo, Paolo Fortina, Anna Rita Virzì, Valeria Pecce, Marialuisa Appetecchia, Alessandra Gentile, Francesca Rosignolo, Melissa Milan, Cosimo Durante, Silvia Benvenuti, Eric Londin, Paolo M. Comoglio, Agnese Barnabei, Marialuisa Sponziello, & Sebastiano Filetti. (2017). Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer. Human Mutation, 39, 371–377. https://doi.org/10.1002/humu.23378

Chicago

Antonella Verrienti, Ferdinando Marandino, Diego Russo, Paolo Fortina, Anna Rita Virzì, Valeria Pecce, Marialuisa Appetecchia, et al. 2017. “Whole Exome Sequencing Identifies a Germline MET Mutation in Two Siblings with Hereditary Wild-Type RET Medullary Thyroid Cancer.” Human Mutation 39 (December): 371–77. doi:10.1002/humu.23378.