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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.
Affiliation
  • Nikasa P; Department of Molecular Medicine, Faculty of Advanced Biomedical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Rabbani B; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
  • Hejazi MS; Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Firouzi A; Department of Molecular Medicine, Faculty of Advanced Biomedical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Baharvand H; Molecular Medicine Research Center, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Totonchi M; Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Mahdieh N; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Clin Pediatr Endocrinol ; 30(4): 201-204, 2021.
Article de En | MEDLINE | ID: mdl-34629743
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Clin Pediatr Endocrinol Année: 2021 Type de document: Article Pays d'affiliation: Iran Pays de publication: Japon
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Clin Pediatr Endocrinol Année: 2021 Type de document: Article Pays d'affiliation: Iran Pays de publication: Japon