| Literature DB >> 30442414 |
Pauline Romanet1, Pascal Philibert2, Frédéric Fina3, Thomas Cuny4, Catherine Roche5, L'houcine Ouafik6, Françoise Paris7, Rachel Reynaud8, Anne Barlier5.
Abstract
The GNAS postzygotic mosaic activating mutations involved in fibrous dysplasia and McCune-Albright syndrome (MAS) are not detectable in leukocytes by Sanger sequencing. Digital droplet polymerase chain reaction detects GNAS mutations in 7 of 12 patients (58.3%) suspected to have fibrous dysplasia/MAS from whole blood DNA, and in 4 of 5 patients (80%) from circulating cell-free DNA.Entities:
Keywords: detection; mosaic mutation; mosaicism
Mesh:
Substances:
Year: 2018 PMID: 30442414 DOI: 10.1016/j.jpeds.2018.09.070
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406