Understanding rare variant contributions to autism: lessons from dystrophin-deficient model

MLA

Claudia Ismania Samogy Costa, et al. “Understanding Rare Variant Contributions to Autism: Lessons from Dystrophin-Deficient Model.” Npj Genomic Medicine, vol. 10, no. 1, Mar. 2025, pp. 1–12. EBSCOhost, https://doi.org/10.1038/s41525-025-00469-5.

APA

Claudia Ismania Samogy Costa, Luciana Madanelo, Jaqueline Yu Ting Wang, Gabriele da Silva Campos, Ana Cristina De Sanctis Girardi, Marília Scliar, Frederico Monfardini, Rita de Cássia Mingroni Pavanello, Vivian Romanholi Cória, Maria Dulcetti Vibranovski, Ana Cristina Krepischi, Naila Cristina Vilaça Lourenço, Mayana Zatz, Guilherme Lopes Yamamoto, Elaine Cristina Zachi, & Maria Rita Passos-Bueno. (2025). Understanding rare variant contributions to autism: lessons from dystrophin-deficient model. Npj Genomic Medicine, 10(1), 1–12. https://doi.org/10.1038/s41525-025-00469-5

Chicago

Claudia Ismania Samogy Costa, Luciana Madanelo, Jaqueline Yu Ting Wang, Gabriele da Silva Campos, Ana Cristina De Sanctis Girardi, Marília Scliar, Frederico Monfardini, et al. 2025. “Understanding Rare Variant Contributions to Autism: Lessons from Dystrophin-Deficient Model.” Npj Genomic Medicine 10 (1): 1–12. doi:10.1038/s41525-025-00469-5.