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Genome Information for Homo sapiens
Graves’ hyperthyroidism (GH) is a common organ-specific autoimmune disease, with an annual incidence of 20 to 50 cases per 100,000 persons.
More...Graves’ hyperthyroidism (GH) is a common organ-specific autoimmune disease, with an annual incidence of 20 to 50 cases per 100,000 persons. Graves’ ophthalmopathy (GO) characterized by disfiguring and dysfunctioning features of proptosis，diplopia or optic neuropathy progress in up to 50% GH patients .
Less...| Accession | PRJNA516279 |
| Data Type | Raw sequence reads |
| Scope | Monoisolate |
| Organism | Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens |
| Submission | Registration date: 21-Jan-2019
The First Affiliated Hospital of Xi'an Jiao Tong University |
| Locus Tag Prefix | ESZ19 |
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