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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:	Mutation-in-Brief
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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