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G Lucotte Selected Research

Deafness (Deaf Mutism)

1/2004Neonatal detection of the 35delG mutation of the GJB2 gene in families at risk for deafness.
2/2001PCR test for diagnosis of the common GJB2 (connexin 26) 35delG mutation on dried blood spots and determination of the carrier frequency in France.

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G Lucotte Research Topics

Disease

2Myositis Ossificans (Fibrodysplasia Ossificans Progressiva)
01/2009 - 01/2007
2Deafness (Deaf Mutism)
01/2004 - 02/2001
1Oculocutaneous albinism type 2
08/2007
1Parkinson Disease (Parkinson's Disease)
04/2004
1Venous Thromboembolism
03/2001
1Multiple Sclerosis
04/2000

Drug/Important Bio-Agent (IBA)

2activin AIBA
01/2009 - 01/2007
1Type 1 Melanocortin ReceptorIBA
08/2007
1Cytochrome P-450 CYP2D6 (CYP2D6)IBA
04/2004
1glutathione S-transferase M1IBA
04/2004
1DNA (Deoxyribonucleic Acid)IBA
01/2004
1factor V LeidenIBA
03/2001
1Connexin 26IBA
02/2001
1CytokinesIBA
04/2000
1Tumor Necrosis Factor-alpha (Tumor Necrosis Factor)IBA
04/2000