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Table 2 Rate of nuclei with prophase-like chromosome (PLC) morphology

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

Designation

Mean [%]

PLC Rate SD [%]

Range [%]

n

MCPH2 Patient

1.36

± 0.5

0.79-2.33

7

Normal Controls

1.17

± 0.85

0-2.09

8

MCPH1 Patients

9.07

± 4.02

5.96-13.77

3

  1. N: number of independent experiments in the reported MCPH2 patient or number of individuals with single experiments in normal and MCPH1 controls.
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Orphanet Journal of Rare Diseases

ISSN: 1750-1172