<--- Back to Details
First PageDocument Content
Kolling / Mitochondrial disease / Human mitochondrial genetics / Mitochondrion / Mutation / Neurogenetics / Mitochondrial DNA / Amyotrophic lateral sclerosis / Biology / Genetics / Kolling Institute of Medical Research
Date: 2009-05-11 22:14:12
Kolling
Mitochondrial disease
Human mitochondrial genetics
Mitochondrion
Mutation
Neurogenetics
Mitochondrial DNA
Amyotrophic lateral sclerosis
Biology
Genetics
Kolling Institute of Medical Research

Molecular solutions to medical problems Issue 30 March[removed]Kolling

Add to Reading List

Source URL: www.kolling.usyd.edu.au

Download Document from Source Website

File Size: 774,00 KB

Share Document on Facebook

Similar Documents

Mitochondrial DNA Part B Resources ISSN: (PrintOnline) Journal homepage: http://www.tandfonline.com/loi/tmdn20 The complete mitochondrial genome of

DocID: 1uck7 - View Document

Mitochondrial DNA (mtDNA) JGSGO June 5, 2018 MtDNA - outline •  What is it?

DocID: 1u1Y4 - View Document

Novel techniques for the prevention of mitochondrial DNA disorders: an ethical review Nuffield Council on Bioethics

DocID: 1tvKZ - View Document

Correlation of microscopic and mitochondrial DNA hair comparisons

DocID: 1t0bz - View Document

Effect of Substratum on the Development and Release of the Triactinomyxon Stage of Myxobolus cerebralis in Mitochondrial DNA 16S Tubifex tubifex Lineages Principal Investigators Dolores V. Baxa, Staff Research Associate,

DocID: 1sDMb - View Document