A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2.
Mozzillo E, Delvecchio M, Carella M, Grandone E, Palumbo P, Salina A, Aloi C, Buono P, Izzo A, D'Annunzio G, Vecchione G, Orrico A, Genesio R, Simonelli F, Franzese A.
Mozzillo E, et al. Among authors: aloi c.
BMC Med Genet. 2014 Jul 24;15:88. doi: 10.1186/1471-2350-15-88.
BMC Med Genet. 2014.
PMID: 25056293
Free PMC article.