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A case of autosomal recessive hypercholesterolemia with a novel mutation in the LDLRAP1 gene

Detalles Bibliográficos
Autores principales: Nikasa, Parisa, Rabbani, Bahareh, Hejazi, Mohammad Saeid, Firouzi, Ata, Baharvand, Hossein, Totonchi, Mehdi, Mahdieh, Nejat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2021
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
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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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