A zebrafish model for FHL1-opathy reveals loss-of-function effects of human FHL1 mutations.

Keßler, M; Kieltsch, A; Kayvanpour, E; Katus, H A; Schoser, B; Schessl, J; Just, S; Rottbauer, W

Keßler, M; Kieltsch, A; Kayvanpour, E; Katus, H A; Schoser, B; Schessl, J; Just, S; Rottbauer, W.

Affiliation

Keßler M; University Hospital of Ulm, Department of Internal Medicine II, Ulm, Germany.
Kieltsch A; University of Ulm, Molecular Cardiology, Department of Internal Medicine II, Ulm, Germany.
Kayvanpour E; University Hospital of Heidelberg, Internal Medicine III, Heidelberg, Germany.
Katus HA; University Hospital of Heidelberg, Internal Medicine III, Heidelberg, Germany.
Schoser B; University Hospital of Munich, Friedrich-Baur-Institut, München, Germany.
Schessl J; University Hospital of Munich, Friedrich-Baur-Institut, München, Germany; Städtisches Klinikum Karlsruhe, Department of Neurology, Karlsruhe, Germany.
Just S; University of Ulm, Molecular Cardiology, Department of Internal Medicine II, Ulm, Germany. Electronic address: steffen.just@uniklinik-ulm.de.
Rottbauer W; University Hospital of Ulm, Department of Internal Medicine II, Ulm, Germany. Electronic address: wolfgang.rottbauer@uniklinik-ulm.de.

Neuromuscul Disord ; 28(6): 521-531, 2018 06.

Article in En | MEDLINE | ID: mdl-29735270

Subject(s)
Key words

FHL1; FHL1-opathy; Loss of function; Myopathy; Zebrafish

Fulltext

Add to My VHL

XML

PubMed Links

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscle, Skeletal / Intracellular Signaling Peptides and Proteins / LIM Domain Proteins / Muscle Proteins / Muscular Diseases / Mutation / Myocardium Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Neuromuscul Disord Journal subject: NEUROLOGIA Year: 2018 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido

Fulltext

Add to My VHL

XML

PubMed Links

Search on Google