APA (7th ed.) Zitazioa

Youssef El Kadiri, Ilham Ratbi, Fatima Zahra Laarabi, Yamna Kriouile, Abdelaziz Sefiani, & Jaber Lyahyai. (2021). Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: A case report. BMC.

Chicago Style (17th ed.) Zitazioa

Youssef El Kadiri, Ilham Ratbi, Fatima Zahra Laarabi, Yamna Kriouile, Abdelaziz Sefiani, eta Jaber Lyahyai. Identification of a Novel LAMA2 C.2217G > A, P.(Trp739*) Mutation in a Moroccan Patient with Congenital Muscular Dystrophy: A Case Report. BMC, 2021.

MLA (9th ed.) Zitazioa

Youssef El Kadiri, et al. Identification of a Novel LAMA2 C.2217G > A, P.(Trp739*) Mutation in a Moroccan Patient with Congenital Muscular Dystrophy: A Case Report. BMC, 2021.