A human immunodeficiency syndrome caused by mutations in CARMIL2.
Schober T, Magg T, Laschinger M, Rohlfs M, Linhares ND, Puchalka J, Weisser T, Fehlner K, Mautner J, Walz C, Hussein K, Jaeger G, Kammer B, Schmid I, Bahia M, Pena SD, Behrends U, Belohradsky BH, Klein C, Hauck F.
Schober T, et al. Among authors: fehlner k.
Nat Commun. 2017 Jan 23;8:14209. doi: 10.1038/ncomms14209.
Nat Commun. 2017.
PMID: 28112205
Free PMC article.