Phenotypic manifestation of homozygous partial deletion of the chromosome 1 segment spanning <i>CFHR3</i> region
This article presents two clinical cases of patients with a homozygous deletion of segment of chromosome 1, which covers regions of genes associated with complement factor H, in particular CFHR3. Patients underwent in-depth clinical studies, heredity assessment, laboratory, instrumental and genetic...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Russo |
| Publicat: |
St. Petersburg branch of the Russian Association of Allergologists and Clinical Immunologists
2020-05-01
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| Col·lecció: | Медицинская иммунология |
| Matèries: | |
| Accés en línia: | https://www.mimmun.ru/mimmun/article/view/1901 |
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