PACS1-Related Syndrome (Schuurs-Hoeijmakers Syndrome)

קרןNational Organization for Rare Disorders
סוגResearch Grants
תאריך אחרון16/07/2018
פקולטהLife Sciences, Medicine

Key features of the PACS1 syndrome are developmental delay (cognitive, language, motor), intellectual disability, and characteristic facial appearance (including hypertelorism with downslanting palpebral fissures, arched eyebrows, bulbous nasal tip, and thin upper lip), due to a mutation in the PACS1 gene. 

The purpose of the NORD Research Grant Program is to encourage meritorious studies designed to improve the diagnosis or therapy of rare "orphan" diseases.


Funding: $45,000 total 
Duration: 2 years


It is expected that one grant will be awarded. 


Research Authority due date: 9.7.18

Preliminary abstract (required) due date: 15.7.18
Full proposal due date: TBD (August 2018)

קבצים מצורפים
עדכון אחרוןעדכון אחרון: 29/05/2018
אוניברסיטת תל-אביב, ת.ד. 39040, תל-אביב 6997801
UI/UX Basch_Interactive