A novel mutation in the matrix metallopeptidase 2 coding gene associated with intrafamilial variability of multicentric osteolysis, nodulosis, and arthropathy

Year of publication

2019

Authors

Kroger, Liisa; Löppönen, Tuija; Ala-Kokko, Leena; Kröger, Heikki; Jauhonen, Hanna-Mari; Lehti, Kaisa; Jaaskelainen, Jarmo

Organizations and authors

University of Eastern Finland

Kröger Heikki

Jääskeläinen Jarmo

Löppönen Tuija

University of Helsinki

Lehti Kaisa

Kuopio University Hospital

Kröger Liisa

Löppönen Tuija

Kröger Heikki

Helsinki University Hospital

Lehti Kaisa

Publication type

Publication format

Article

Parent publication type

Journal

Article type

Original article

Audience

Scientific

Peer-reviewed

Peer-Reviewed

MINEDU's publication type classification code

A1 Journal article (refereed), original research

Publication channel information

Journal/Series

Molecular genetics & genomic medicine

Parent publication name

Molecular Genetics & Genomic Medicine

Volume

Issue

Pages

e802

ISSN

2324-9269

Publication forum

82670

Publication forum level

Open access

Open access in the publisher’s service

Yes

Open access of publication channel

Fully open publication channel

Self-archived

Yes

License of the self-archived publication

CC BY

Other information

Fields of science

Genetics, developmental biology, physiology; Biomedicine; General medicine, internal medicine and other clinical medicine

Keywords

[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

Internationality of the publisher

International

Language

English

International co-publication

Yes

Co-publication with a company

DOI

10.1002/mgg3.802

The publication is included in the Ministry of Education and Culture’s Publication data collection

Yes