APA (7th ed.) Citation

Nectoux, J., Heron, D., Tallot, M., Chelly, J., & Bienvenu, T. (2006). Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome. Clinical Genetics, 70(1), 29. https://doi.org/10.1111/j.1399-0004.2006.00629.x

Chicago Style (17th ed.) Citation

Nectoux, J., D. Heron, M. Tallot, J. Chelly, and T. Bienvenu. "Maternal Origin of a Novel C-terminal Truncation Mutation in CDKL5 Causing a Severe Atypical Form of Rett Syndrome." Clinical Genetics 70, no. 1 (2006): 29. https://doi.org/10.1111/j.1399-0004.2006.00629.x.

MLA (9th ed.) Citation

Nectoux, J., et al. "Maternal Origin of a Novel C-terminal Truncation Mutation in CDKL5 Causing a Severe Atypical Form of Rett Syndrome." Clinical Genetics, vol. 70, no. 1, 2006, p. 29, https://doi.org/10.1111/j.1399-0004.2006.00629.x.