To build a collaborative network of health care providers and scientists to decode the molecular underpinnings and understand the extent of rare genetic and bone marrow failure disorders in India.
By identifying the genetic cause of rare genetic diseases and bone marrow failure syndromes and unraveling the underlying disease biology, we aspire to provide new and innovative insights leading to improved targeted therapeutic options for patients
"The establishment of the rare genetic and bone marrow disorder consortium is a great initiative that will further intensify the ongoing collaboration between Ghent and Nitte University"
Director, Centre for Medical Genetics, Ghent University, Belgium
"The establishment of the rare genetic and bone marrow disorder consortium is a great initiative that will further intensify the ongoing collaboration between Ghent and Nitte University"
Director, Centre for Medical Genetics, Ghent University, Belgium
Bringing together clinicians and researchers under one platform to improve clinical therapies and outcomes for the patients.
