Work

Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene (ACTA1) mutation

Year: 2010

Type: article

Study design: Case Report

Source: Neuromuscular Disorders

DOI: 10.1016/j.nmd.2010.06.008

Authors: Werner Stenzel, Stefan Prokop, Wolfram Kress, Stephanie Huppmann, Andrea Loui, Nanette M.E. Sarioglu, Nigel G. Laing, John C. Sparrow, Frank L. Heppner, Hans H. Goebel

Institutions: Charité – Universitätsmedizin Berlin, University of Würzburg, Stiftung Charité, The University of Western Australia, Harry Perkins Institute of Medical Research, University of York, Johannes Gutenberg University Mainz

Language: English

Topic: Muscle Physiology and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: National Health and Medical Research Council

Award: Uncoupled Research Fellowship

OpenAlex ID: W1981984468

FWCI: 0.521

Cites: 17

Cited by: 13

Related to: 10