Novel de novo mutations inZBTB20in Primrose syndrome with congenital hypothyroidism
about
The integration site of the APP transgene in the J20 mouse model of Alzheimer's disease.A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing.Toward clinical and molecular understanding of pathogenic variants in the ZBTB18 gene.Alterations in metabolic patterns have a key role in diagnosis and progression of primrose syndrome.Molecular Genetics of Pigment Dispersion Syndrome and Pigmentary Glaucoma: New Insights into Mechanisms.
P2860
Novel de novo mutations inZBTB20in Primrose syndrome with congenital hypothyroidism
description
im April 2016 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 07 April 2016
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована у квітні 2016
@uk
name
Novel de novo mutations inZBTB20in Primrose syndrome with congenital hypothyroidism
@en
Novel de novo mutations inZBTB20in Primrose syndrome with congenital hypothyroidism
@nl
type
label
Novel de novo mutations inZBTB20in Primrose syndrome with congenital hypothyroidism
@en
Novel de novo mutations inZBTB20in Primrose syndrome with congenital hypothyroidism
@nl
prefLabel
Novel de novo mutations inZBTB20in Primrose syndrome with congenital hypothyroidism
@en
Novel de novo mutations inZBTB20in Primrose syndrome with congenital hypothyroidism
@nl
P2093
P2860
P356
P1476
Novel de novo mutations in ZBTB20 in Primrose syndrome with congenital hypothyroidism
@en
P2093
Andrea Superti-Furga
Bénédicte Gérard
Francesca Mattioli
Sheila Unger
P2860
P304
P356
10.1002/AJMG.A.37645
P407
P577
2016-04-07T00:00:00Z