Literature DB >> 29878396

Genotype-Phenotype Correlation of PLOD2 Skeletal Dysplasias Using Structural Information.

Emma Tham1,2, Gintautas Grigelionis2, Anna Hammarsjö1,2, Giedre Grigelioniene1,2.   

Abstract

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 29878396     DOI: 10.1002/jbmr.3460

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


× No keyword cloud information.
  1 in total

1.  Case Report: Exome Sequencing Identified a Novel Compound Heterozygous Variation in PLOD2 Causing Bruck Syndrome Type 2.

Authors:  Jing Zhang; Huaying Hu; Weihong Mu; Mei Yu; Wenqi Chen; Dongqing Mi; Kai Yang; Qing Guo
Journal:  Front Genet       Date:  2021-02-16       Impact factor: 4.599

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.