Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies.
Brue T, Quentien MH, Khetchoumian K, Bensa M, Capo-Chichi JM, Delemer B, Balsalobre A, Nassif C, Papadimitriou DT, Pagnier A, Hasselmann C, Patry L, Schwartzentruber J, Souchon PF, Takayasu S, Enjalbert A, Van Vliet G, Majewski J, Drouin J, Samuels ME.
Brue T, et al. Among authors: bensa m.
BMC Med Genet. 2014 Dec 19;15:139. doi: 10.1186/s12881-014-0139-9.
BMC Med Genet. 2014.
PMID: 25524009
Free PMC article.