Shaheen R et al. Mutations in TMEM231 cause Meckel–Gruber syndrome. J Med Genet. 2013;50(3):160-2. PMID: 23349226.
Srour M et al. Mutations in TMEM231 cause Joubert syndrome in French Canadians. J Med Genet. 2012;49(10):636-41. PMID: 23012439.
TMEM231