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1750-1172-8-178
1750-1172-8-178
http://dx.doi.org/10.1186/1750-1172-8-178
Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation
P356
Q34479346-E278B77F-1437-4E02-B68F-75C7FCDA3B2F
P356
1750-1172-8-178
http://dx.doi.org/10.1186/1750-1172-8-178