Khuller, K. Et Al. 2021. MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.10 .

Khuller, K., Yigit, G., Grijalva, C. M., Altmueller, J., Thiele, H., Nurnberg, P., ... Elcioglu, N. H.(2021). MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.10.

Khuller, Katharina Et Al. "MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease," EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.10, 2021

Khuller, Katharina Et Al. "MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.10, 2021

Khuller, K. Et Al. (2021) . "MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.10.

@article{article, author={Katharina Khuller Et Al. }, title={MFSD2A-associated primary microcephaly-Expanding the clinical and mutational spectrum of this ultra-rare disease}, journal={EUROPEAN JOURNAL OF MEDICAL GENETICS}, year=2021}