7p21.3 Together With a 12p13.32 Deletion in a Patient With Microcephaly-Does 12p13.32 Locus Possibly Comprises a Candidate Gene Region for Microcephaly?

Martina Rincic; Milan Rados; Janja Kopic; Zeljka Krsnik; Thomas Liehr

doi:10.3389/fnmol.2021.613091

7p21.3 Together With a 12p13.32 Deletion in a Patient With Microcephaly-Does 12p13.32 Locus Possibly Comprises a Candidate Gene Region for Microcephaly?

Front Mol Neurosci. 2021 Feb 4:14:613091. doi: 10.3389/fnmol.2021.613091. eCollection 2021.

Authors

Martina Rincic¹, Milan Rados¹, Janja Kopic¹, Zeljka Krsnik¹, Thomas Liehr²

Affiliations

¹ Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Zagreb, Croatia.
² Jena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Jena, Germany.

No abstract available

Keywords: PRMT8; array comparative genetic hybridization (aCGH); intellectual disability—genetics*; magnetic resonace imaging (MRI); microcephaly.

Grants and funding

WT_/Wellcome Trust/United Kingdom