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Accession: PRJEB9519 ID: 285768

Homo sapiens (human)

MT-CO1 mutations in POI patients

See Genome Information for Homo sapiens
Primary ovarian insufficiency (POI) is a syndrome of amenorrhea, sex steroid deficiency and elevated gonadotropins in women younger than 40 years. More...
AccessionPRJEB9519
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 3-Jun-2015
- Chinese Academy of Sciences
- Jianbo Lu
Locus Tag PrefixBN1872
Project Data:
No public data is linked to this project. Any recently released data that cites this project will be linked to it within a few days.

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