Résultat correspond à votre recherche
-
Source :
Genes Immun.2003 avr 30Pmid / DOI:
12215906 -
Leber congenital amaurosis--genotyping required for possible inclusion in a clinical trial.
Isabelle PERRAULT, Jean-Michel Rozet, Arnold Munnich
Source :
Adv Exp Med Biol2003 jan 1Pmid / DOI:
15180249 -
The ABCA4 gene in autosomal recessive cone-rod dystrophies.
Jean-Michel Rozet, Arnold Munnich
Source :
Am J Hum Genet2002 déc 1Pmid / DOI:
12515255 -
Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness.
Sylvain Ernest
Source :
Hum. Mol. Genet.2000 nov 21Pmid / DOI:
10958658 -
Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity.
Source :
Science1995 juin 29Pmid / DOI:
7539157 -
Digitoxin metabolism by rat liver microsomes.
Source :
Biochem. Pharmacol.1976 jan 23Pmid / DOI:
https://doi.org/10.1016/0006-2952(75)90094-5 -
Atomic models for the polypeptide backbones of myohemerythrin and hemerythrin.
Source :
Biochem Biophys Res Commun1975 oct 27Pmid / DOI:
Impaired eIF5A function causes -
Source :
Wiley Interdiscip Rev Syst Biol Med0000 jan 1Pmid / DOI:
25286050 -
Lydie Burglen
Source :
Genet Med.Pmid / DOI:
32103185 -
Neuroinflammatory disorders and mastocytosis: A possible association?
Olivier Hermine
Source :
J Allergy Clin Immunol PractPmid / DOI:
31077881 -
Omalizumab Therapy for Mast Cell-Mediator Symptoms in Patients with ISM, CM, MMAS, and MCAS.
Laurent Frenzel, Olivier Hermine
Source :
J Allergy Clin Immunol PractPmid / DOI:
30954641
