| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/NG1110-923 |
| P698 | PubMed publication ID | 20980985 |
| P50 | author | Bernd Wollnik | Q28324741 |
| P2860 | cites work | Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations | Q24296941 |
| Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture | Q24301645 | ||
| WDR62 is associated with the spindle pole and is mutated in human microcephaly | Q24301673 | ||
| Primary microcephaly: do all roads lead to Rome? | Q33629131 | ||
| Cell-cycle control and cortical development | Q34630030 | ||
| Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options | Q37080467 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | microcephaly | Q431643 |
| P304 | page(s) | 923-924 | |
| P577 | publication date | 2010-11-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | A common mechanism for microcephaly | |
| P478 | volume | 42 |
| Q57809058 | A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis |
| Q35321786 | A novel single base pair duplication in WDR62 causes primary microcephaly |
| Q24315121 | CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly |
| Q28973602 | CPAP promotes timely cilium disassembly to maintain neural progenitor pool |
| Q40225704 | Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders |
| Q91437140 | Genomic and phenotypic delineation of congenital microcephaly |
| Q90634984 | MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis |
| Q24317320 | Microcephaly-associated protein WDR62 regulates neurogenesis through JNK1 in the developing neocortex |
| Q28577785 | Molecular and cellular insights into Zika virus-related neuropathies |
| Q34035966 | Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly |
| Q35029169 | Opposing roles for JNK and Aurora A in regulating the association of WDR62 with spindle microtubules. |
| Q38116442 | Recent advances in the genetic etiology of brain malformations |
| Q35664162 | Reciprocal Relationship between Head Size, an Autism Endophenotype, and Gene Dosage at 19p13.12 Points to AKAP8 and AKAP8L |
| Q31149019 | The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome |
| Q110764725 | WITHDRAWN: Novel pathogenic mutation mapping of ASPM gene in consanguineous Pakistani families with primary microcephaly |
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