MSeqDR. The mtDNA and mitochondrial disease tool and data resource!
MSeqDR. The mtDNA and mitochondrial disease tool and data resource!
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(CBSNEWS) — In what experts are calling a “revolutionary” medical event, the first baby with DNA from three parents has been born. The little boy, now nearly six months old, was conceived using a controversial technique meant to help people who carry...
Researchers examine disease-causing mutations in mitochondrial genomes Researchers examine disease-causing mutations in mitochondrial genomes By Kyle Davis ScM Candidate, Genetic Counseling, JHU/NHGRI The study of genetic disease has often centered...
Download citric acid and power EBooks | Read online citric acid and power EBooks Citric Acid Biotechnology, This work covers citric acid fermentation methods including recent advances and approaches. The book looks at all aspects of the fermentation...
Our fortnightly round-up up of news from the Wellcome Trust community… Vaccination combats severe diarrhoea in Malawi Research published in Lancet Infectious Diseases has found that the introduction of a rotavirus vaccine in Malawi has significantly...
A five-month-old boy is the first baby to be born using a new technique that incorporates DNA from three people, according to New Scientist. The child was born to Ibtisam Shaban and Mahmoud Hassan, from Jordan, who had been trying to start a family...
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Submit new data - MSeqDR-LSDB Mitochondrial Disease Locus Specific Database
MSeqDR-LSDB Mitochondrial Disease Locus Specific Database If you are not registered as a submitter, please do so here.
View disease #00012 - MSeqDR-LSDB Mitochondrial Disease Locus Specific Database
- This is a placeholder individual (patient) entry for enabling quick variant submission without finishing all details about an individual. Please create true individual entries as soon as possible, i...
MSeqDR ~ Accelerating Genomic Discovery in Mitochondrial Diseases
This is MSeqDR.org, the mtDNA and mitochondrial disease tool and data resource, using NGS and clinical data to do exome, genome and pathogenic variant interpretation.
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