Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene

Year of publication

2018

Authors

Lehtokari, Vilma-Lotta; Gardberg, Maria; Pelin, Katarina; Wallgren-Pettersson, Carina

Organizations and authors

University of Turku

Gardberg Maria

University of Helsinki

Wallgren-Pettersson Carina

Pelin Katarina

Lehtokari Vilma-Lotta

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

Volume

Issue

Pages

323-326

ISSN

0960-8966

Publication forum

63906

Publication forum level

Open access

Open access in the publisher’s service

Open access of publication channel

Partially open publication channel

Self-archived

Yes

Other information

Fields of science

Biomedicine; General medicine, internal medicine and other clinical medicine

Keywords

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

Publication country

United Kingdom

Internationality of the publisher

International

Language

English

International co-publication

Co-publication with a company

DOI

10.1016/j.nmd.2017.12.009

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

Yes