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Article

MFSD2A-associated primary microcephaly - expanding the clinical and mutational spectrum of this ultra-rare disease.
Khuller, K. ORCID logoORCID: https://orcid.org/0000-0003-4765-0572, Yigit, G., Martínez Grijalva, C. ORCID logoORCID: https://orcid.org/0000-0002-0901-376X, Altmüller, J. ORCID logoORCID: https://orcid.org/0000-0003-4372-1521, Thiele, H., Nürnberg, P., Elcioglu, N.H., Yeter, B. ORCID logoORCID: https://orcid.org/0000-0002-6255-1057, Hehr, U., Stein, A., Della Marina, A., Köninger, A., Depienne, C., Kaiser, F.J., Wollnik, B. and Kuechler, A.
European Journal of Medical Genetics 64 (10): 104310. October 2021

Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation.
Posch, M.G., Boldt, L.H., Polotzki, M., Richter, S., Rolf, S., Perrot, A. ORCID logoORCID: https://orcid.org/0000-0002-8800-342X, Dietz, R., Oezcelik, C. and Haverkamp, W.
European Journal of Medical Genetics 53 (4): 201-203. July 2010

Review

Improved molecular platform for the gene therapy of rare diseases by liver protein secretion.
Quiviger, M., Giannakopoulos, A., Verhenne, S., Marie, C., Stavrou, E.F., Vanhoorelbeke, K., Izsvák, Z. ORCID logoORCID: https://orcid.org/0000-0002-2053-2384, De Meyer, S.F., Athanassiadou, A. and Scherman, D.
European Journal of Medical Genetics 61 (11): 723-728. November 2018

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