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A case of autosomal recessive hypercholesterolemia with a novel mutation in the LDLRAP1 gene
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society for Pediatric Endocrinology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481080/ https://www.ncbi.nlm.nih.gov/pubmed/34629743 http://dx.doi.org/10.1297/cpe.30.201 |
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author | Nikasa, Parisa Rabbani, Bahareh Hejazi, Mohammad Saeid Firouzi, Ata Baharvand, Hossein Totonchi, Mehdi Mahdieh, Nejat |
author_facet | Nikasa, Parisa Rabbani, Bahareh Hejazi, Mohammad Saeid Firouzi, Ata Baharvand, Hossein Totonchi, Mehdi Mahdieh, Nejat |
author_sort | Nikasa, Parisa |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-8481080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Japanese Society for Pediatric Endocrinology |
record_format | MEDLINE/PubMed |
spelling | pubmed-84810802021-10-08 A case of autosomal recessive hypercholesterolemia with a novel mutation in the LDLRAP1 gene Nikasa, Parisa Rabbani, Bahareh Hejazi, Mohammad Saeid Firouzi, Ata Baharvand, Hossein Totonchi, Mehdi Mahdieh, Nejat Clin Pediatr Endocrinol Mutation-in-Brief The Japanese Society for Pediatric Endocrinology 2021-10-01 2021 /pmc/articles/PMC8481080/ /pubmed/34629743 http://dx.doi.org/10.1297/cpe.30.201 Text en 2021©The Japanese Society for Pediatric Endocrinology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Mutation-in-Brief Nikasa, Parisa Rabbani, Bahareh Hejazi, Mohammad Saeid Firouzi, Ata Baharvand, Hossein Totonchi, Mehdi Mahdieh, Nejat A case of autosomal recessive hypercholesterolemia with a novel mutation in the LDLRAP1 gene |
title | A case of autosomal recessive hypercholesterolemia with a novel mutation in
the LDLRAP1 gene |
title_full | A case of autosomal recessive hypercholesterolemia with a novel mutation in
the LDLRAP1 gene |
title_fullStr | A case of autosomal recessive hypercholesterolemia with a novel mutation in
the LDLRAP1 gene |
title_full_unstemmed | A case of autosomal recessive hypercholesterolemia with a novel mutation in
the LDLRAP1 gene |
title_short | A case of autosomal recessive hypercholesterolemia with a novel mutation in
the LDLRAP1 gene |
title_sort | case of autosomal recessive hypercholesterolemia with a novel mutation in
the ldlrap1 gene |
topic | Mutation-in-Brief |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8481080/ https://www.ncbi.nlm.nih.gov/pubmed/34629743 http://dx.doi.org/10.1297/cpe.30.201 |
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