Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non‐syndromic rod‐cone dystrophy.

MLA

Méjécase, Cécile, et al. “Whole Exome Sequencing Resolves Complex Phenotype and Identifies CC2D2A Mutations Underlying Non‐syndromic Rod‐cone Dystrophy.” Clinical Genetics, vol. 95, no. 2, Feb. 2019, pp. 329–33. EBSCOhost, https://doi.org/10.1111/cge.13453.

APA

Méjécase, C., Hummel, A., Mohand, S. S., Andrieu, C., El Shamieh, S., Antonio, A., Condroyer, C., Boyard, F., Foussard, M., Blanchard, S., Letexier, M., Saraiva, J., Sahel, J., Zeitz, C., & Audo, I. (2019). Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non‐syndromic rod‐cone dystrophy. Clinical Genetics, 95(2), 329–333. https://doi.org/10.1111/cge.13453

Chicago

Méjécase, Cécile, Aurélie Hummel, Saïd, Saddek Mohand, Camille Andrieu, Said El Shamieh, Aline Antonio, Christel Condroyer, et al. 2019. “Whole Exome Sequencing Resolves Complex Phenotype and Identifies CC2D2A Mutations Underlying Non‐syndromic Rod‐cone Dystrophy.” Clinical Genetics 95 (2): 329–33. doi:10.1111/cge.13453.