Rodan, L. H., Spillmann, R. C., Kurata, H. T., Lamothe, S. M., Maghera, J., Jamra, R. A., … Shashi, V. (2021). Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations. Genet Med, 23(10), 2016. https://doi.org/10.1038/s41436-021-01306-7

Rodan, Lance H., Rebecca C. Spillmann, Harley T. Kurata, Shawn M. Lamothe, Jasmine Maghera, Rami Abou Jamra, Anna Alkelai, et al. “Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.” Genet Med 23, no. 10 (October 2021): 2016. https://doi.org/10.1038/s41436-021-01306-7.

Rodan LH, Spillmann RC, Kurata HT, Lamothe SM, Maghera J, Jamra RA, et al. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations. Genet Med. 2021 Oct;23(10):2016.

Rodan, Lance H., et al. “Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.” Genet Med, vol. 23, no. 10, Oct. 2021, p. 2016. Pubmed, doi:10.1038/s41436-021-01306-7.

Rodan LH, Spillmann RC, Kurata HT, Lamothe SM, Maghera J, Jamra RA, Alkelai A, Antonarakis SE, Atallah I, Bar-Yosef O, Bilan F, Bjorgo K, Blanc X, Van Bogaert P, Bolkier Y, Burrage LC, Christ BU, Granadillo JL, Dickson P, Donald KA, Dubourg C, Eliyahu A, Emrick L, Engleman K, Gonfiantini MV, Good J-M, Kalser J, Kloeckner C, Lachmeijer G, Macchiaiolo M, Nicita F, Odent S, O’Heir E, Ortiz-Gonzalez X, Pacio-Miguez M, Palomares-Bralo M, Pena L, Platzer K, Quinodoz M, Ranza E, Rosenfeld JA, Roulet-Perez E, Santani A, Santos-Simarro F, Pode-Shakked B, Skraban C, Slaugh R, Superti-Furga A, Thiffault I, van Jaabrsveld RH, Vincent M, Wang H-G, Zacher P, Undiagnosed Diseases Network, Rush E, Pitt GS, Au PYB, Shashi V. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations. Genet Med. 2021 Oct;23(10):2016.