# Proprotein convertase subtilisin/kexin 9 V4I variant with LDLR mutations modifies the phenotype of familial hypercholesterolemia

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/proprotein-convertase-subtilisin-kexin-9-v4i-variant-with-ldlr-mutations/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Naotaka Ohta,Mika Hori,Atsushi Takahashi,Masatsune Ogura,Hisashi Makino,Tamiko Tamanaha,Hiromi Fujiyama,Yoshihiro Miyamoto,Mariko Harada‐Shiba |
| Citations | 56 |
| DOI | 10.1016/j.jacl.2015.12.024 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2227136327 |
| PMID | 27206942 |
| Type | article |
| Year | 2016 |

## Paper authors

- [Tamiko Tamanaha](https://scholariq.org/researchers/tamiko-tamanaha/)

## Paper journal

- [Journal of clinical lipidology](https://scholariq.org/journals/journal-of-clinical-lipidology/)

## Paper primary topic

- [Lipoproteins and Cardiovascular Health](https://scholariq.org/topics/lipoproteins-and-cardiovascular-health/)

## Paper topics

- [Lipoproteins and Cardiovascular Health](https://scholariq.org/topics/lipoproteins-and-cardiovascular-health/)
- [Diabetes, Cardiovascular Risks, and Lipoproteins](https://scholariq.org/topics/diabetes-cardiovascular-risks-and-lipoproteins/)
- [Dermatological and Skeletal Disorders](https://scholariq.org/topics/dermatological-and-skeletal-disorders/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.