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Publications by M Zatz
The p.P56S Mutation in theVAPBgene Is Not Due to a Single Founder: The First European Case
Clinical Genetics
Genetics
Analysis of the Serotonin Transporter Polymorphism (5-Httlpr) in Brazilian Patients Affected by Dysthymia, Major Depression and Bipolar Disorder
Molecular Psychiatry
Psychiatry
Molecular Neuroscience
Mental Health
Molecular Biology
Cellular
The Association of the Short Variant of the 5-HTTPLR Polymorphism and the apoE4 Allele Does Not Increase the Risk for Late Onset Alzheimer’s Disease
Molecular Psychiatry
Psychiatry
Molecular Neuroscience
Mental Health
Molecular Biology
Cellular
A First Missense Mutation in the Delta Sarcoglycan Gene Associated With a Severe Phenotype and Frequency of Limb-Girdle Muscular Dystrophy Type 2F (LGMD2F) in Brazilian Sarcoglycanopathies.
Journal of Medical Genetics
Genetics
How the Magnitude of Clinical Severity and Recurrence Risk Affects Reproductive Decisions in Adult Males With Different Forms of Progressive Muscular Dystrophy.
Journal of Medical Genetics
Genetics
Further Evidence for the Organisation of the Four Sarcoglycans Proteins Within the Dystrophin–glycoprotein Complex
European Journal of Human Genetics
Genetics
