HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Arnaud Pj Giese Selected Research

Autosomal Recessive 26 Deafness

1/2018Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.

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:


Arnaud Pj Giese Research Topics

Disease

1Usher Syndromes (Usher Syndrome)
11/2021
1Deafness (Deaf Mutism)
01/2018
1Autosomal Recessive 26 Deafness
01/2018

Drug/Important Bio-Agent (IBA)

1Proto-Oncogene Proteins c-metIBA
01/2018
1MethyltransferasesIBA
01/2018
1Carrier Proteins (Binding Protein)IBA
01/2018

Therapy/Procedure

1Therapeutics
11/2021