IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients-Reference-Cited by-同舟云学术

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IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients

Published:2019-06-03 Issue:1 Volume:13 Page:
ISSN:1479-7364
Container-title:Human Genomics
language:en
Short-container-title:Hum Genomics

Author:

Zhytnik Lidiia^ORCID,Maasalu Katre,Duy Binh Ho,Pashenko Andrey,Khmyzov Sergey,Reimann Ene,Prans Ele,Kõks Sulev,Märtson Aare

Funder

Estonian Ministry of Education and Research

H2020 ERA-chair grant

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1186/s40246-019-0209-3.pdf

Reference46 articles.

1. Byers PH, Steiner RD. Osteogenesis imperfecta. Annu Rev Med. 1992;43:269–82.

2. Van Dijk FS, Pals G, Van Rijn RR, Nikkels PGJ, Cobben JM. Classification of Osteogenesis Imperfecta revisited. Eur J Med Genet. 2010;53:1–5.

3. Rauch F, Glorieux F. Osteogenesis imperfecta. Lancet. 2004;363(9418):1377–85.

4. Sillence DO, Senn A, Danks DM. Genetic heterogeneity in osteogenesis imperfecta. J Med Genet. 1979;16:101–16.

5. Fratzl-Zelman N, Misof BM, Roschger P, Klaushofer K. Classification of osteogenesis imperfecta. Wien Med Wochenschr. 2015;165:264–70.

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4. IFITM3 Promotes Osteogenic Differentiation of Human Dental Pulp Stem Cells by Modulating MAPK Signaling;Journal of Hard Tissue Biology;2023

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