A. Zecha

发表

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Wei Chen, Reinhard Ullmann, Dagmar Wieczorek, 2011, Nature.

Cerebral haemorrhagic infarction in young patients with hereditary protein C deficiency: evidence for "spontaneous" cerebral venous thrombosis.

G. Bots, A. Wintzen, E. Briët, 1985, British medical journal.

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots

H. Ropers, D. Wieczorek, A. Tzschach, 2011, Human Genetics.

CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling.

Marco Y. Hein, J. Gécz, S. Lenzner, 2013, The Journal of clinical investigation.