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Publications by John R. Mills
Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates With Unique Phenotype
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology
Mitochondrion-Dependent N-Terminal Processing of Outer Membrane McL-1 Protein Removes an Essential Mule/Lasu1 Protein-Binding Site
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Hereditary Renal Amyloidosis With a Variant Lysozyme p.Trp82Arg in a Chinese Family: Case Report and Literature Review
BMC Nephrology
Nephrology
First Report of Hereditary Lysozyme Amyloidosis in a South Asian Family
Case Reports in Hematology
Hereditary ATTR Amyloidosis With Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)
Internal Medicine
Internal Medicine
Medicine
Identifying Mixed Phenotype: Evaluating the Presence of Polyneuropathy in Patients With Hereditary Transthyretin-Mediated Amyloidosis With Cardiomyopathy
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology
Diagnostic Challenges in Hereditary Transthyretin Amyloidosis With Polyneuropathy: Avoiding Misdiagnosis of a Treatable Hereditary Neuropathy
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Brain Transcriptomic Analysis of Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type
Frontiers in Aging Neuroscience
Aging
Cognitive Neuroscience
Typing of Hereditary Renal Amyloidosis Presenting With Isolated Glomerular Amyloid Deposition
BMC Nephrology
Nephrology
A Patient With Hereditary ATTR and a Novel AGel p.Ala578Pro Amyloidosis
Mayo Clinic Proceedings
Medicine
Identification of a New Hereditary Amyloidosis Prealbumin Variant, Tyr-77, and Detection of the Gene by DNA Analysis.
Journal of Clinical Investigation
Medicine
