Cacciagli, P., Sutera-Sardo, J., Borges-Correia, A., Roux, J., Dorboz, I., Desvignes, J., . . . Villard, L. (2013). Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus. Elsevier.
Style de citation ChicagoCacciagli, Pierre, et al. Mutations in BCAP31 Cause a Severe X-Linked Phenotype With Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus. Elsevier, 2013.
Style de citation MLACacciagli, Pierre, et al. Mutations in BCAP31 Cause a Severe X-Linked Phenotype With Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus. Elsevier, 2013.
Attention : ces citations peuvent ne pas être correctes à 100%.