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Abnormal centrosome and spindle morphology in a patient wit..:
Farag, Heba Gamal
;
Froehler, Sebastian
;
Oexle, Konrad
...
Orphanet Journal of Rare Diseases. 8 (2013) 1 - p. , 2013
Link:
https://doi.org/10.1186/1750-1172-8-178
RT Journal T1
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_1750-1172-8-178&Exemplar=1&LAN=DE A1 Farag, Heba Gamal A1 Froehler, Sebastian A1 Oexle, Konrad A1 Ravindran, Ethiraj A1 Schindler, Detlev A1 Staab, Timo A1 Huebner, Angela A1 Kraemer, Nadine A1 Chen, Wei A1 Kaindl, Angela M PB Springer Science and Business Media LLC YR 2013 SN 1750-1172 JF Orphanet Journal of Rare Diseases VO 8 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/1750-1172-8-178 DO https://doi.org/10.1186/1750-1172-8-178 SF ELIB - SuUB Bremen
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