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Article

The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued.
Schröder, S., Yigit, G., Li, Y., Altmüller, J., Büttel, H.M., Fiedler, B., Kretzschmar, C., Nürnberg, P., Seeger, J., Serpieri, V., Valente, E.M., Wollnik, B., Boltshauser, E. and Brockmann, K.
Orphanet Journal of Rare Diseases 18 (1): 101. 2 May 2023

Comparison of zebrafish and mice knockouts for Megalencephalic Leukoencephalopathy proteins indicates that GlialCAM/MLC1 forms a functional unit.
Pérez-Rius, C., Folgueira, M., Elorza-Vidal, X., Alia, A., Hoegg-Beiler, M.B., Eeza, M.N.H., Díaz, M.L., Nunes, V., Barrallo-Gimeno, A. and Estévez, R.
Orphanet Journal of Rare Diseases 14 (1): 268. 21 November 2019

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutations.
Farag, H.G., Froehler, S., Oexle, K., Ravindran, E., Schindler, D., Staab, T., Huebner, A., Kraemer, N., Chen, W. and Kaindl, A.M.
Orphanet Journal of Rare Diseases 8 (1): 178. 14 November 2013

Letter

Combined immunodeficiency develops with age in immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2).
von Bernuth, H., Ravindran, E., Du, H., Froehler, S., Strehl, K., Kraemer, N., Issa-Jahns, L., Amulic, B., Ninnemann, O., Xiao, M.S., Eirich, K., Koelsch, U., Hauptmann, K., John, R., Schindler, D., Wahn, V., Chen, W. and Kaindl, A.M.
Orphanet Journal of Rare Diseases 9 (1): 116. 21 October 2014