Molecular Review of Suspected Alport Syndrome Patients—A Single-Centre Experience
Paulina Halat(Children's Memorial Health Institute), Krystyńa Chrzańowska(University Medical Center Groningen), Rafał Płoski(Medical University of Warsaw), Grażyna Kostrzewa(Medical University of Warsaw), Piotr Stawiński(Medical University of Warsaw), Katarzyna Iwanicka‐Pronicka(Children's Memorial Health Institute), Elżbieta Ciara(Children's Memorial Health Institute), Mieczysław Litwin(Children's Memorial Health Institute), Michał Pac(Children's Memorial Health Institute), Ewelina Bielska(Children's Memorial Health Institute), Beata Chałupczyńska(Children's Memorial Health Institute), Łukasz Obrycki(Children's Memorial Health Institute), Dorota Siestrzykowska(Children's Memorial Health Institute), Dorota Wicher(Children's Memorial Health Institute)
Cited by 9
Related Papers
2016 European Society of Hypertension guidelines for the management of high blood pressure in children and adolescents
|Journal of Hypertension|2016|1.4k
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
|The American Journal of Human Genetics|2005|562
Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia
|Journal of the American Society of Nephrology|2015|284
New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre
|Journal of Translational Medicine|2016|233