Pernicious Anaemia and Hypoparathyroidism in a Patient with Kearns-Sayre Syndrome with Mitochondrial DNA Duplication

Overview

Journal J Inherit Metab Dis

Publisher Wiley

Date 1996 Jan 1

PMID 8739941

Authors

M J Abramowicz

P Cochaux

L H Cohen

E Vamos

Affiliations

Soon will be listed here.

References

Rotig A, Bessis J, Romero N, Cormier V, Saudubray J, Narcy P . Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia. Am J Hum Genet. 1992; 50(2):364-70. PMC: 1682469. View

HORWITZ S, ROESSMANN U . Kearns-Sayre syndrome with hypoparathyroidism. Ann Neurol. 1978; 3(6):513-8. DOI: 10.1002/ana.410030611. View

Poulton J, Holt I . Mitochondrial DNA: does more lead to less?. Nat Genet. 1994; 8(4):313-5. DOI: 10.1038/ng1294-313. View

Aaltonen J, Bjorses P, Sandkuijl L, Perheentupa J, Peltonen L . An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21. Nat Genet. 1994; 8(1):83-7. DOI: 10.1038/ng0994-83. View