Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia-Reference-Cited by-同舟云学术

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Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia

Published:2004 Issue:5 Volume:24 Page:439-440
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Mabuchi Akihiko,Haga Nobuhiko,Maeda Koichi,Nakashima Eiji,Manabe Noriyo,Hiraoka Hisatada,Kitoh Hiroshi,Kosaki Rika,Nishimura Gen,Ohashi Hirofumi,Ikegawa Shiro

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 48 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The favorable outcome of Bernese periacetabular osteotomy for the hip osteoarthritis in multiple epiphyseal dysplasia;Orphanet Journal of Rare Diseases;2023-10-30

2. Designing a risk prognosis model based on natural killer cell-linked genes to accurately evaluate the prognosis of gastric cancer;BIOCELL;2023

3. Identification of MATN3 as a Novel Prognostic Biomarker for Gastric Cancer through Comprehensive TCGA and GEO Data Mining;Disease Markers;2021-12-02

4. Matrilin-3-Primed Adipose-Derived Mesenchymal Stromal Cell Spheroids Prevent Mesenchymal Stromal-Cell-Derived Chondrocyte Hypertrophy;International Journal of Molecular Sciences;2020-11-24

5. A novel homozygous missense variant in MATN3 causes spondylo-epimetaphyseal dysplasia Matrilin 3 type in a consanguineous family;European Journal of Medical Genetics;2020-08

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