Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutations.
| Autor: | Farag, Heba Gamal1 drhebagamal@yahoo.com, Froehler, Sebastian2 sebastian.froehler@mdc-berlin.de, Oexle, Konrad3 oexle@humangenetik.med.tum.de, Ravindran, Ethiraj4 ethiraj.ravindran@charite.de, Schindler, Detlev5 schindler@biozentrum.uni-wuerzburg.de, Staab, Timo6 timo.staab@uni-wuerzburg.de, Huebner, Angela1 angela.huebner@uniklinikum-dresden.de, Kraemer, Nadine1 nadine.kraemer@charite.de, Chen, Wei1 wei.chen@mdc-berlin.de, Kaindl, Angela M.1 angela.kaindl@charite.de |
|---|---|
| Zdroj: | Orphanet Journal of Rare Diseases. 2013, Vol. 8 Issue 1, p1-27. 26p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
|