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Publications by Hans H Goebel

In-Frame Deletion in the Seventh Immunoglobulin-Like Repeat of Filamin C in a Family With Myofibrillar Myopathy

European Journal of Human Genetics

English

Related publications

A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy

American Journal of Human Genetics

English

Skeletal Myopathy in a Family With Lamin a/C Cardiac Disease

Cardiovascular Diagnosis and Therapy

Cardiovascular Medicine

English

Deletion of the Ste20-Like Kinase SLK in Skeletal Muscle Results in a Progressive Myopathy and Muscle Weakness

Skeletal Muscle

Sports Medicine

Molecular Biology

English

Reducing Bodies and Myofibrillar Myopathy Features in FHL1 Muscular Dystrophy

English

Cystic Fibrosis Transmembrane Conductance Regulator Interacts With Multiple Immunoglobulin Domains of Filamin A

Journal of Biological Chemistry

Molecular Biology

English

Construction of Chromosomal In-Frame Deletion Mutants in Rhodobacter Capsulatus

English

A Family With Liddle's Syndrome Caused by a New C.1721 Deletion Mutation in the Epithelial Sodium Channel Β‑subunit

Experimental and Therapeutic Medicine

Cancer Research

English

Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy

Molecular Neuroscience

English

Reporting a Rare Form of Myopathy, Myopathy With Extrapyramidal Signs, in an Iranian Family Using Next Generation Sequencing: A Case Report

BMC Medical Genetics

English