Alazami, A. M., Adly, N., Al Dhalaan, H., & Alkuraya, F. S. (2011). A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18). Springer-Verlag.
Style de citation ChicagoAlazami, Anas M., Nouran Adly, Hisham Al Dhalaan, et Fowzan S. Alkuraya. A Nullimorphic ERLIN2 Mutation Defines a Complicated Hereditary Spastic Paraplegia Locus (SPG18). Springer-Verlag, 2011.
Style de citation MLAAlazami, Anas M., Nouran Adly, Hisham Al Dhalaan, et Fowzan S. Alkuraya. A Nullimorphic ERLIN2 Mutation Defines a Complicated Hereditary Spastic Paraplegia Locus (SPG18). Springer-Verlag, 2011.
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