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Publications by Snaevar Sigurdsson
Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated With a Defect in the Autophagy Gene Encoding RAB24
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
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Hereditary Spastic Paraplegia SPG13 Is Associated With a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
American Journal of Human Genetics
Genetics
The Clinical Course and Genetic Defect in the PCFT Gene in a 27-Year-Old Woman With Hereditary Folate Malabsorption
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
A Polymorphism in the Gene Encoding CART Is Not Associated With Obesity in Pima Indians
International Journal of Obesity
Nutrition
Endocrinology
Dietetics
Medicine
Metabolism
Diabetes
A Novel Mutation in CELSR1 Is Associated With Hereditary Lymphedema
Vascular Cell
Computer Networks
Developmental Neuroscience
Neurology
Cell Biology
Communications
Hereditary Ataxia and Spastic Paraplegia in Portugal
JAMA Neurology
Neurology
A Case of Friedreich's Hereditary Ataxia: With Necropsy
BMJ
Hereditary Episodic Ataxia
Quantum and Classical Integrable Sine-Gordon Model With Defect
Nuclear Physics B
High Energy Physics
Nuclear
The V122I Mutation in Hereditary Transthyretin-Mediated Amyloidosis Is Significantly Associated With Polyneuropathy
Journal of Cardiac Failure
Cardiovascular Medicine
Cardiology