A case of autosomal recessive hypercholesterolemia with a novel mutation in the LDLRAP1 gene.
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ABSTRACT:
SUBMITTER: Nikasa P
PROVIDER: S-EPMC8481080 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature
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A case of autosomal recessive hypercholesterolemia with a novel mutation in the <i>LDLRAP1</i> gene.
Nikasa Parisa P Rabbani Bahareh B Hejazi Mohammad Saeid MS Firouzi Ata A Baharvand Hossein H Totonchi Mehdi M Mahdieh Nejat N
Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 20211001 4
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