Linda Xu

A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome

V. Steen, O. Bruland, G. Houge, 2018, European Journal of Human Genetics.

Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome.

Julie C. Sapp, L. Biesecker, J. Johnston, 2018, American journal of human genetics.

Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene.

M. Gorry, T. Hart, J. Sandhu, 2003, Kidney international.

A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome

V. Steen, O. Bruland, G. Houge, 2018, European Journal of Human Genetics.