Andersen-tawil syndrome presenting with complete heart block

K Suetterlin, R Männikkö, E Flossmann… - Journal of …, 2021 - content.iospress.com
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant neuromuscular disorder due
to mutations in the KCNJ2 gene. The classical phenotype of ATS consists of a triad of …

Andersen-Tawil Syndrome Presenting with Complete Heart Block

K Suetterlin, R Männikkö, E Flossmann… - Journal of …, 2021 - eprints.ncl.ac.uk
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant neuromuscular disorder due
to mutations in the KCNJ2 gene. The classical phenotype of ATS consists of a triad of …

Andersen-Tawil Syndrome Presenting with Complete Heart Block

K Suetterlin, R Männikkö, E Flossmann… - Journal of …, 2021 - discovery.ucl.ac.uk
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant neuromuscular disorder due
to mutations in the KCNJ2 gene. The classical phenotype of ATS consists of a triad of …

Andersen-Tawil Syndrome Presenting with Complete Heart Block.

K Suetterlin, R Männikkö, E Flossmann… - Journal of …, 2021 - europepmc.org
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant neuromuscular disorder due
to mutations in the KCNJ2 gene. The classical phenotype of ATS consists of a triad of …

Andersen-Tawil Syndrome Presenting with Complete Heart Block

K Suetterlin, R Männikkö… - Journal of …, 2021 - pubmed.ncbi.nlm.nih.gov
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant neuromuscular disorder due
to mutations in the KCNJ2 gene. The classical phenotype of ATS consists of a triad of …

Andersen-Tawil Syndrome Presenting with Complete Heart Block

K Suetterlin, R Männikkö, E Flossmann… - J Neuromuscul …, 2021 - openaccess.sgul.ac.uk
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant neuromuscular disorder due
to mutations in the KCNJ2 gene. The classical phenotype of ATS consists of a triad of …

Andersen-Tawil Syndrome Presenting with Complete Heart Block

K Suetterlin, R Männikkö, E Flossmann… - J Neuromuscul …, 2021 - openaccess.sgul.ac.uk
Andersen-Tawil syndrome (ATS) is a rare autosomal dominant neuromuscular disorder due
to mutations in the KCNJ2 gene. The classical phenotype of ATS consists of a triad of …