Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6042463 | Pediatric Neurology | 2013 | 7 Pages |
Abstract
We propose that the disorder is caused by the more conserved mutation p.Thr186Arg, with the second sequence change identified, p.Pro416His, possibly further negatively affecting the function of the protein. However, it is unclear which of the two changes, or maybe both, represents the causative mutation. A single missense mutation in TAF2 in a family with microcephaly and intellectual disability was described in a large-scale study reporting on the identification of 50 novel genes. We suggest that a mutation in TAF2 can cause this syndrome.
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Authors
Shlomit MSc, Pola MSc, Ayelet MD, Metsada PhD, Adva MSc, Adi MSc, Idit MD, Rachel MD, Dvir MSc, Ami PhD, Mordechai MD, Lina MD, PhD,