Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation

因复合杂合 WDR62 基因突变导致的常染色体隐性原发性小头畸形 2 型患者的着丝粒和纺锤体形态异常