APA (7th ed.) Citation

Feda E. Mohamed, Mohammad A. Ghattas, Mohammad A. Ghattas, Taleb M. Almansoori, Mohammed Tabouni, Ibrahim Baydoun, . . . Fatma Al-Jasmi. (2023). Novel compound heterozygous variants (c.971delA/c.542C > T) in SLC1A4 causes spastic tetraplegia, thin corpus callosum, and progressive microcephaly: A case report and mutational analysis. Frontiers Media S.A..

Chicago Style (17th ed.) Citation

Feda E. Mohamed, et al. Novel Compound Heterozygous Variants (c.971delA/c.542C > T) in SLC1A4 Causes Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly: A Case Report and Mutational Analysis. Frontiers Media S.A., 2023.

MLA (9th ed.) Citation

Feda E. Mohamed, et al. Novel Compound Heterozygous Variants (c.971delA/c.542C > T) in SLC1A4 Causes Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly: A Case Report and Mutational Analysis. Frontiers Media S.A., 2023.