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Mutations inNFKB2and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies
Brue, Thierry, Quentien, Marie-Hélène, Khetchoumian, Konstantin, Bensa, Marco, Capo-Chichi, José-Mario, Delemer, Brigitte, Balsalobre, Aurelio, Nassif, Christina, Papadimitriou, Dimitris T, Pagnier, AVolume:
15
Langue:
english
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-014-0139-9
Date:
December, 2014
Fichier:
PDF, 1.17 MB
english, 2014