HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

G Brochier Selected Research

congenital Microcoria

5/2017A novel gain-of-function mutation in ORAI1 causes late-onset tubular aggregate myopathy and congenital miosis.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown:


G Brochier Research Topics

Disease

1congenital Microcoria
05/2017
1Blood Platelet Disorders (Thrombocytopathy)
05/2017
1Arthrogryposis
12/2008
1Nemaline Myopathies (Nemaline Myopathy)
12/2008
1Cap Myopathy
12/2008
1Muscular Diseases (Myopathy)
12/2008
1Cystic Fibrosis (Mucoviscidosis)
05/2000
1Infections
05/2000

Drug/Important Bio-Agent (IBA)

1Calcium Release Activated Calcium ChannelsIBA
05/2017
1Creatine Kinase (Creatine Phosphokinase)IBA
05/2017
1TropomyosinIBA
12/2008
1Type III Secretion SystemsIBA
05/2000