Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report.Published in:2018By:Berrani, H.;Meskini, T.;Zerkaoui, M.;Merhni, H.;Ettair, S.;Sefiani, A.;Mouane, N.Publication type:journal article
Elevated IgM levels as a marker for a unique phenotype in patients with Ataxia telangiectasia.Published in:2018By:Krauthammer, Alexander;Lahad, Avishay;Goldberg, Lior;Sarouk, Ifat;Weiss, Batia;Somech, Raz;Soudack, Michalle;Pessach, Itai M.Publication type:journal article