Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia-Reference-Cited by-同舟云学术

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Identification of a Novel De Novo COMP Gene Variant as a Likely Cause of Pseudoachondroplasia

Published:2021-02-15 Issue:7 Volume:29 Page:546-550
ISSN:1541-2016
Container-title:Applied Immunohistochemistry & Molecular Morphology
language:en
Short-container-title:

Author:

Tuncel Gulten,Akcan Nese,Gul Seref,Sag Sebnem O.,Bundak Ruveyde,Mocan Gamze,Temel Sehime G.,Ergoren Mahmut C.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Medical Laboratory Technology,Histology,Pathology and Forensic Medicine

Reference19 articles.

1. Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia;Hecht;Nat Genet,1995

2. Pseudoachondroplasia and multiple epiphyseal dysplasia: mutation review, molecular interactions, and genotype to phenotype correlations;Briggs;Hum Mutat,2002

3. Comparative protein structure modeling using MODELLER;Webb;Curr Protoc Bioinformatics,2016

4. Comparative protein structure modeling of genes and genomes;Marti-Renom;Annu Rev Biophys Biomol Struct,2000

5. Computational methods for predicting protein-protein interactions using various protein features;Ding;Curr Protoc Protein Sci,2018

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