Wolfram syndrome 2: a novel CISD2 mutation identified in Italian siblings.

Authors :: Rondinelli M
Novara F
Calcaterra V
Zuffardi O
Genovese S
Source :: Acta diabetologica [Acta Diabetol] 2015 Feb; Vol. 52 (1), pp. 175-8. Date of Electronic Publication: 2014 Nov 05.
Publication Year :: 2015

Subjects :: Adult
Base Sequence
Female
Humans
Introns
Italy
Molecular Sequence Data
Young Adult
Aging, Premature genetics
Hearing Loss, Sensorineural genetics
Membrane Proteins genetics
Mitochondrial Diseases genetics
Mutation
Optic Atrophy genetics

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