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Publications by Jason Ensor
Liddle’s Syndrome in an African Male Due to a Novel Frameshift Mutation in the Beta-Subunit of the Epithelial Sodium Channel Gene
Cardiovascular Journal of Africa
Medicine
Cardiovascular Medicine
Cardiology
Related publications
The Diagnosis of Liddle Syndrome by Identification of a Mutation in the Beta Subunit of the Epithelial Sodium Channel.
Journal of Medical Genetics
Genetics
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
Medicine
Cancer Research
Immunology
Microbiology
Slow‐channel Myasthenia Due to Novel Mutation in M2 Domain of AChR Delta Subunit
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
Rapp-Hodgkin and AEC Syndromes Due to a New Frameshift Mutation in the TP63 Gene
Journal of Medical Genetics
Genetics
Identification of a Novel Frameshift Mutation in PITX2 Gene in a Chinese Family With Axenfeld-Rieger Syndrome
Journal of Zhejiang University: Science B
Genetics
Pharmacology
Molecular Biology
Biochemistry
Veterinary
Medicine
Toxicology
Pharmaceutics
Identification of a Single Cytosine Base Insertion Mutation at Arg-597 of the Beta Subunit of the Human Epithelial Sodium Channel in a Family With Liddle's Disease
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
A Rare Cause of Primary Hypoparathyroidism Due to a Novel Mutation in the GATA3 Gene – The Barakat Syndrome
International Journal of Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
A Novel Frameshift Mutation in the XPC Gene in a Moroccan Patient: A Case Report
Journal of Medical Case Reports
Medicine
Novel Deletion Mutation in the Cardiac Sodium Channel Inactivation Gate Causes Long QT Syndrome
International Journal of Cardiology
Cardiovascular Medicine
Cardiology
