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Resource Name
Mayo Mitochondrial Disease Biobank
RRID:SCR_010598 RRID Copied      
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Mayo Mitochondrial Disease Biobank (RRID:SCR_010598)
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Resource Information

URL: http://mayoresearch.mayo.edu/mitochondrial-disease-biobank/

Proper Citation: Mayo Mitochondrial Disease Biobank (RRID:SCR_010598)

Description: A biobank of blood and tissue samples from patients with known and suspected mitochondrial diseases along with data from their families. Samples are used in research to understand the family of mitochondrial disorders such as Alpers' syndrome, encephalopathy, and Friedrieich's ataxia, among many others. The goal of the biobank is to advance the understanding of mitochondrial disease and improve patient care.

Abbreviations: Mitochondrial Biobank

Synonyms: Mayo Clinic Mitochondrial Disease Biobank, Mitochondrial Disease Biobank

Resource Type: biomaterial supply resource, cell repository, material resource

Keywords: blood, tissue, mitochondrial disease, mitochrondrial disorder, alper's progressive sclerosing polio dystrophy, leber hereditary optic neuroretinopathy, barth syndrome, leigh syndrome, leigh-like syndrome, chronic progressive external ophthalmoplegia, mitochondrial myopathy, encephalopathy, lactic acidosis, stroke-like episodes, melas, dominant optic atrophy, myoclonic epilepsy associated with ragged-red fibers, merrf, merrf syndrome, friedreich's ataxia, neuropathy ataxia, retinitis pigmentosa, narp, hereditary paragangliom, pearson syndrome, hereditary spastic paraplegia, wolfram syndrome, kearns-sayre syndrome, research, biobank, treatment, patient care

Related Condition: Mitochondrial disease, Mitochrondrial disorder, Alper's progressive sclerosing poliodystrophy, Leber hereditary optic neuroretinopathy, Barth syndrome, Leigh syndrome, Leigh-like Syndrome, Chronic progressive exteRNAl ophthalmoplegia, Mitochondrial myopathy, Encephalopathy, Lactic acidosis, Stroke-like episodes, MELAS, Dominant optic atrophy, Myoclonic epilepsy associated with ragged-red fibers, MERRF Syndrome, Friedreich's Ataxia, Neuropathy ataxia and retinitis pigmentosa, Hereditary paragangliom, Pearson syndrome, Hereditary spastic paraplegia, Wolfram syndrome, Kearns-Sayre syndrome

Availability: Available to the research community, Application and review process

Resource Name: Mayo Mitochondrial Disease Biobank

Resource ID: SCR_010598

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Data and Source Information

Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400