A New Type of Mitochondrial DNA Deletion in Patients with Encephalomyopathy

Overview

Journal J Inherit Metab Dis

Publisher Wiley

Date 1991 Jan 1

PMID 1779627

Citations 2

Authors

S Miyabayashi

H Hanamizu

H Endo

K Tada

S Horai

Affiliations

Soon will be listed here.

Citing Articles

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).

Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, OHTOMO M Diabetologia. 1994; 37(8):818-25.

PMID: 7988784 DOI: 10.1007/BF00404339.

3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.

Klopstock T, Bischof F, Gerok K, Deuschl G, Seibel P, Ketelsen U Acta Neuropathol. 1995; 90(2):126-9.

PMID: 7484086 DOI: 10.1007/BF00294310.

References

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