CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR
Clinical case of a patient with family hypercholesterolemia caused by mutation c.1859G>C (p.W620S) in the gene of human low density lipoproteins receptor.
| Main Authors: | , , , , , , , , |
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| Format: | Article |
| Language: | Russian |
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«SILICEA-POLIGRAF» LLC
2015-12-01
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| Series: | Кардиоваскулярная терапия и профилактика |
| Online Access: | https://cardiovascular.elpub.ru/jour/article/view/282 |
| _version_ | 1827063847176896512 |
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| author | V. A. Korneva T. Yu. Kuznetsova T. Yu. Bogoslovskaya R. Z. Murtazina A. V. Didio M. P. Serebrenitskaya V. O. Konstantinov M. Yu. Mandelshtam V. B. Vasiliev |
| author_facet | V. A. Korneva T. Yu. Kuznetsova T. Yu. Bogoslovskaya R. Z. Murtazina A. V. Didio M. P. Serebrenitskaya V. O. Konstantinov M. Yu. Mandelshtam V. B. Vasiliev |
| author_sort | V. A. Korneva |
| collection | DOAJ |
| description | Clinical case of a patient with family hypercholesterolemia caused by mutation c.1859G>C (p.W620S) in the gene of human low density lipoproteins receptor. |
| first_indexed | 2024-04-10T03:36:30Z |
| format | Article |
| id | doaj.art-a43422fb12344776a864c9543e81a2e3 |
| institution | Directory Open Access Journal |
| issn | 1728-8800 2619-0125 |
| language | Russian |
| last_indexed | 2025-03-19T22:37:45Z |
| publishDate | 2015-12-01 |
| publisher | «SILICEA-POLIGRAF» LLC |
| record_format | Article |
| series | Кардиоваскулярная терапия и профилактика |
| spelling | doaj.art-a43422fb12344776a864c9543e81a2e32024-10-17T12:21:34Zrus«SILICEA-POLIGRAF» LLCКардиоваскулярная терапия и профилактика1728-88002619-01252015-12-01146525310.15829/1728-8800-2015-6-52-53277CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTORV. A. Korneva0T. Yu. Kuznetsova1T. Yu. Bogoslovskaya2R. Z. Murtazina3A. V. Didio4M. P. Serebrenitskaya5V. O. Konstantinov6M. Yu. Mandelshtam7V. B. Vasiliev8Petrozavodsk State University, PetrozavodskPetrozavodsk State University, PetrozavodskFSBSI “Institute of Experimental Medicine”, Saint-PetersburgFSBSI “Institute of Experimental Medicine”, Saint-Petersburg; Saint-Petersburg State University, Saint-PetersburgFSBSI “Institute of Experimental Medicine”, Saint-Petersburg; Saint-Petersburg State University, Saint-PetersburgI.I. Mechnikov North-West State Medical University, Saint-PetersburgI.I. Mechnikov North-West State Medical University, Saint-PetersburgFSBSI “Institute of Experimental Medicine”, Saint-Petersburg; Saint-Petersburg State University, Saint-PetersburgFSBSI “Institute of Experimental Medicine”, Saint-Petersburg; Saint-Petersburg State University, Saint-PetersburgClinical case of a patient with family hypercholesterolemia caused by mutation c.1859G>C (p.W620S) in the gene of human low density lipoproteins receptor.https://cardiovascular.elpub.ru/jour/article/view/282 |
| spellingShingle | V. A. Korneva T. Yu. Kuznetsova T. Yu. Bogoslovskaya R. Z. Murtazina A. V. Didio M. P. Serebrenitskaya V. O. Konstantinov M. Yu. Mandelshtam V. B. Vasiliev CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR Кардиоваскулярная терапия и профилактика |
| title | CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR |
| title_full | CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR |
| title_fullStr | CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR |
| title_full_unstemmed | CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR |
| title_short | CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR |
| title_sort | clinical case of a patient with family hypercholesterolemia caused by mutation c 1859g c p w620s in the gene of human low density lipoproteins receptor |
| url | https://cardiovascular.elpub.ru/jour/article/view/282 |
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