Understanding SETBP1 Science

Understanding SETBP1 Science

SETBP1 Genetics: Bite-Sized Breakthroughs

Breaking down new breakthroughs in SETBP1 research in an easy to digest way
Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling
Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling
SETBP1 haploinsufficiency and related disorders clinical and neurobehavioral phenotype study
SETBP1 haploinsufficiency and related disorders clinical and neurobehavioral phenotype study
Speech and language deficits are central to SETBP1 haploinsufficiency disorder
Speech and language deficits are central to SETBP1 haploinsufficiency disorder

 

Clinical delineation of SETBP1 haploinsufficiency disorder
Clinical delineation of SETBP1 haploinsufficiency disorder
Genetic architecture of childhood speech disorder: a review
Genetic architecture of childhood speech disorder: a review

 

SETBP1 Science Bites

In this educational series, you will learn about all things SETBP1 in bite-size chunks.
What is SETBP1-HD? – part of the SETBP1 Science Bites educational series presented by Jordan Whitlock, PhD – the newest member of our Medical and Scientific Advisory Board
Variants in SETBP1-HD – part of the SETBP1 Science Bites educational series presented by Jordan Whitlock, PhD – the newest member of our Medical and Scientific Advisory Board