Article Versions Notes

Okutman Ö, Demirel C, Tülek F, Pfister V, Büyük U, Muller J, Charlet-Berguerand N, Viville S. Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect. Genes. 2020; 11(4):382. https://doi.org/10.3390/genes11040382

Okutman, Özlem, Cem Demirel, Firat Tülek, Veronique Pfister, Umut Büyük, Jean Muller, Nicolas Charlet-Berguerand, and Stéphane Viville. 2020. "Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect" Genes 11, no. 4: 382. https://doi.org/10.3390/genes11040382

Okutman, Ö., Demirel, C., Tülek, F., Pfister, V., Büyük, U., Muller, J., Charlet-Berguerand, N., & Viville, S. (2020). Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect. Genes, 11(4), 382. https://doi.org/10.3390/genes11040382