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Orphanet J Rare Dis
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutations
- H.G. Farag
- S. Froehler
- K. Oexle
- E. Ravindran
- D. Schindler
- T. Staab
- A. Huebner
- N. Kraemer
- W. Chen
- A.M. Kaindl