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Mitochondrial diseases
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1	What are mitochondria? Mitochondria are often called the ‘cell’s powerhouse.’ They are specialized compartments within almost every cell. They are responsible for producing 90% of the energy needed by our body to s Add to Reading List Source URL: www.umdf.org Language: English - Date: 2012-07-13 15:28:19 Mitochondrial diseases Mitochondrial genetics Molecular biology Mitochondrion Mitochondrial DNA Genetic disorder Human mitochondrial genetics MELAS syndrome
2	Microsoft Word - 3 R.S.R. Add to Reading List Source URL: www.ata.org.tn Language: English - Date: 2011-02-22 05:31:54 Nonsyndromic deafness Biology Genetics Sensorineural hearing loss Health GJB2 GJB6 Philosophy of biology Mutation Deafness Mitochondrial diseases Channelopathy
3	Facts About Genetics and Neuromuscular Diseases Add to Reading List Source URL: www.mda.org Language: English - Date: 2011-10-03 18:31:08 Mitochondrial disease Mitochondrion Non-Mendelian inheritance Mutation Mitochondrial DNA Human genome Chromosome Duchenne muscular dystrophy Genetic testing Biology Genetics Genetic disorder
4	Preventing incurable genetic disease Mitochondrial replacement offers a route to the prevention of life-limiting genetic disease. However, this procedure involves manipulations of traditional genetic inheritance. It has Add to Reading List Source URL: www.ccc.ox.ac.uk Language: English - Date: 2015-02-17 12:13:17 Organelles Genetics Genetic disorder Mitochondrial diseases Biology Cellular respiration Mitochondrion
5	Q&A: Mitochondrial Donation About 1 in 200 children in the UK carry a mitochondrial DNA mutation, while around 1 in 6500 children is thought to develop serious mitochondrial disease. The Wellcome Trust Centre for Mitocho Add to Reading List Source URL: www.newcastle-mitochondria.com Language: English - Date: 2014-02-28 03:33:55 DNA Spindle transfer Mitochondrial diseases Genetic genealogy Mitochondrion Mitochondrial DNA Human Fertilisation and Embryology Authority Mitochondrial Eve Cell Biology Genetics Mitochondrial genetics
6	Understanding the Genetics of Deafness A Guide for Patients and Families Harvard Medical School Add to Reading List Source URL: hearing.harvard.edu Language: English - Date: 2014-08-13 15:38:18 Deafness Cytogenetics Syndromes Mitochondrial diseases X-linked recessive inheritance Sex linkage Nonsyndromic deafness Usher syndrome Sensorineural hearing loss Biology Genetics Philosophy of biology
7	Medical frontier: Debating mitochondria replacement Annex VI: Patient focus group Report to HFEA February 2013 Add to Reading List Source URL: www.opm.co.uk Language: English - Date: 2014-02-21 11:42:12 Medical genetics Mitochondrial diseases Mitochondrial genetics DNA Mitochondrion Spindle transfer Mitochondrial DNA MELAS syndrome Preimplantation genetic diagnosis Biology Genetics Fertility medicine
8	Microsoft PowerPoint - Website, Rare Disease Day 2012_englisch.ppt Add to Reading List Source URL: www.mh-hannover.de Language: English - Date: 2012-03-01 10:41:42 POLG Mitochondrion Mitochondrial DNA Ataxia MELAS syndrome Genetics Biology Mitochondrial diseases
9	Introduction Hearing is a complex process, so it should be no surprise that the causes of hearing loss are also complex. Hearing loss can occur because of damage to the ear, especially the inner ear. For example, infants Add to Reading List Source URL: hearing.harvard.edu Language: English - Date: 2003-04-23 12:04:19 Deafness Syndromes Medical genetics Mitochondrial diseases X-linked recessive inheritance Sensorineural hearing loss Mutation Chromosome 13 Usher syndrome Genetics Biology Health
10	Deafness genetic mutation discovered Add to Reading List Source URL: medicalxpress.com Language: English - Date: 2015-03-03 23:13:06 Mitochondrial diseases Channelopathy Genetic genealogy Nonsyndromic deafness Syndromes Usher syndrome Stereocilia Wolfram syndrome Usher 1C Genetics Deafness Health

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