Khalaf, G.; Mattern, C.; Begou, M.; Boespflug-Tanguy, O.; Massaad, C.; Massaad-Massade, L.
Mutation of Proteolipid Protein 1 Gene: From Severe Hypomyelinating Leukodystrophy to Inherited Spastic Paraplegia. Biomedicines 2022, 10, 1709.
https://doi.org/10.3390/biomedicines10071709
AMA Style
Khalaf G, Mattern C, Begou M, Boespflug-Tanguy O, Massaad C, Massaad-Massade L.
Mutation of Proteolipid Protein 1 Gene: From Severe Hypomyelinating Leukodystrophy to Inherited Spastic Paraplegia. Biomedicines. 2022; 10(7):1709.
https://doi.org/10.3390/biomedicines10071709
Chicago/Turabian Style
Khalaf, Guy, Claudia Mattern, Mélina Begou, Odile Boespflug-Tanguy, Charbel Massaad, and Liliane Massaad-Massade.
2022. "Mutation of Proteolipid Protein 1 Gene: From Severe Hypomyelinating Leukodystrophy to Inherited Spastic Paraplegia" Biomedicines 10, no. 7: 1709.
https://doi.org/10.3390/biomedicines10071709
APA Style
Khalaf, G., Mattern, C., Begou, M., Boespflug-Tanguy, O., Massaad, C., & Massaad-Massade, L.
(2022). Mutation of Proteolipid Protein 1 Gene: From Severe Hypomyelinating Leukodystrophy to Inherited Spastic Paraplegia. Biomedicines, 10(7), 1709.
https://doi.org/10.3390/biomedicines10071709