Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD).

Author:

Pilz D,Quarrell O W,Jones E W

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference22 articles.

1. Diabetes mellitus and simple optic atrophy amongst siblings;Wolfram, D.J.; Wagner, H.P.

2. Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram synrome);Cremers, C.W.R.J.; Vijdeveld, P.G.A.B.; Pinkers, A.J.L.G.;Acta Paediatr Scand Suppi,1977

3. The Wolfram syndrome: a primary degenerative disorder with lethal potential;Kinsey, B.T.; Firth, R.G.F.;Irish Med J,1992

4. Thiamine responsive anaemia in DIDMOAD syndrome;Borgna-Pignatti, C.; Marradi, P.; Pinelli, L.; Monetti, N.; Patrini, C.;J Pediatr,1989

5. Diabetes mellitus, diabetes insipidus and optic atrophy: an autosomal recessive syndrome?;Fraser, F.C.; Gunn, T.;J Med Genet,1977

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