Lacramioara Fabian

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 6

Top Topics

Muscular Dystrophy

Top Venues

Human molecular genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Lacramioara Fabian, Esmat Karimi, Gerrie P Farman, Jochen Gohlke, Coen A C Ottenheijm, Hendrikus L Granzier, James E Dowling
Comprehensive phenotypic characterization of an allelic series of zebrafish models of NEB-related nemaline myopathy. Human molecular genetics 33 (12) (2024)
Lacramioara Fabian, Esmat Karimi, Gerrie P Farman, Jochen Gohlke, Coen A C Ottenheijm, Hendrikus L Granzier, James E Dowling
Comprehensive phenotypic characterization of an allelic series of zebrafish models of NEB-related nemaline myopathy. Human molecular genetics 33 (12) (2024)
Lacramioara Fabian, Esmat Karimi, Gerrie P Farman, Jochen Gohlke, Coen A C Ottenheijm, Hendrikus L Granzier, James E Dowling
Comprehensive phenotypic characterization of an allelic series of zebrafish models of NEB-related nemaline myopathy. Human molecular genetics 33 (12) (2024)
Lacramioara Fabian, Esmat Karimi, Gerrie P Farman, Jochen Gohlke, Coen A C Ottenheijm, Hendrikus L Granzier, James E Dowling
Comprehensive phenotypic characterization of an allelic series of zebrafish models of NEB-related nemaline myopathy. Human molecular genetics 33 (12) (2024)
Lacramioara Fabian, Esmat Karimi, Gerrie P Farman, Jochen Gohlke, Coen A C Ottenheijm, Hendrikus L Granzier, James E Dowling
Comprehensive phenotypic characterization of an allelic series of zebrafish models of NEB-related nemaline myopathy. Human molecular genetics (2024)
Sarah J Smith, Lacramioara Fabian, Adeel Sheikh, Ramil Noche, Xiucheng Cui, Steven A Moore, James E Dowling
Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophy. Human molecular genetics (2021)