Identical Large Scale Rearrangement of Mitochondrial DNA Causes Kearns-Sayre Syndrome in a Mother and Her Son

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.40.11.858
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

Mitochondrial DNA, Diabetes and Pancreatic Pathology in Kearns-Sayre Syndrome

Diabetologia
Internal MedicineEndocrinologyMetabolismDiabetes
1995English

Progressive Increase of the Mutated Mitochondrial DNA Fraction in Kearns-Sayre Syndrome

Pediatric Research
Child HealthPediatricsPerinatology
1990English

Classical Triad of Kearns-Sayre Syndrome

BMJ Case Reports
Medicine
2016English

Cochlear Implantation in a Patient With Mitochondrial Disease. Kearns-Sayre Syndrome. A Case Report.

Practica Otologica
Otorhinolaryngology
1996English

Mitochondrial DNA Deletion Diagnosed by Analysis of an Endomyocardial Biopsy Specimen From a Patient With Kearns-Sayre Syndrome and Complete Heart Block

Heart
Cardiovascular MedicineCardiology
1992English

Malignant Melanoma of the Choroid in a Mother and Retinoblastoma in Her Son.

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
1986English

CHILD Syndrome in a Mother and Her Daughter : A Case Report

Journal of the Royal Medical Services
2015English

Mitochondrial DNA Deletion in "Identical" Twin Brothers

Journal of Medical Genetics
Genetics
2004English

Phenotype of FOXP2 Haploinsufficiency in a Mother and Son

American Journal of Medical Genetics, Part A
Genetics
2011English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy