Homozygous variants in AMPD2 and COL11A1 lead to a complex phenotype of pontocerebellar hypoplasia type 9 and Stickler syndrome type 2.

MLA

Abreu, Nicolas J., et al. “Homozygous Variants in AMPD2 and COL11A1 Lead to a Complex Phenotype of Pontocerebellar Hypoplasia Type 9 and Stickler Syndrome Type 2.” American Journal of Medical Genetics. Part A, vol. 182, no. 3, Mar. 2020, pp. 557–60. EBSCOhost, https://doi.org/10.1002/ajmg.a.61452.

APA

Abreu, N. J., Koboldt, D. C., Gastier, F. J. M., Dave, W. A., Flanigan, K. M., & Waldrop, M. A. (2020). Homozygous variants in AMPD2 and COL11A1 lead to a complex phenotype of pontocerebellar hypoplasia type 9 and Stickler syndrome type 2. American Journal of Medical Genetics. Part A, 182(3), 557–560. https://doi.org/10.1002/ajmg.a.61452

Chicago

Abreu, Nicolas J., Daniel C. Koboldt, Foster, Julie M. Gastier, Wala, Ashita Dave, Kevin M. Flanigan, and Megan A. Waldrop. 2020. “Homozygous Variants in AMPD2 and COL11A1 Lead to a Complex Phenotype of Pontocerebellar Hypoplasia Type 9 and Stickler Syndrome Type 2.” American Journal of Medical Genetics. Part A 182 (3): 557–60. doi:10.1002/ajmg.a.61452.