Leigh map: A novel computational diagnostic resource for mitochondrial disease-Reference-Cited by-同舟云学术

Leigh map: A novel computational diagnostic resource for mitochondrial disease

Published:2017-01 Issue:1 Volume:81 Page:9-16
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Rahman Joyeeta¹,Noronha Alberto²,Thiele Ines²,Rahman Shamima¹³

Affiliation:

1. Mitochondrial Research Group, Genetics and Genomic Medicine Programme, UCL Great Ormond Street Institute of Child Health; London United Kingdom

2. Luxembourg Center for Systems Biomedicine; University of Luxembourg; Esch-sur-Alzette Luxembourg

3. Mitochondrial Research Group, Genetics and Genomic Medicine Programme, UCL Great Ormond Street Institute of Child Health and Metabolic Department, Great Ormond Street Hospital NHS Foundation Trust; London United Kingdom

Funder

British Inherited Metabolic Disease Group

Luxembourg National Research Fund

Great Ormond Street Hospital Children's Charity

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference23 articles.

1. Mutations causing mitochondrial disease: what is new and what challenges remain?;Lightowlers;Science,2015

2. Whole exome sequencing of suspected mitochondrial patients in clinical practice;Wortmann;J Inherit Metab Dis,2015

3. Leigh syndrome: one disorder, more than 75 monogenic causes;Lake;Ann Neurol,2016

4. Leigh syndrome: clinical features and biochemical and DNA abnormalities;Rahman;Ann Neurol,1996

5. Subacute necrotizing encephalomyelopathy in an infant;Leigh;J Neurol Neurosurg Psychiatry,1951

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