Debrisoquine Hydroxylase Gene Polymorphism in Familial Parkinson's Disease.

Journal of Neurology, Neurosurgery and Psychiatry- United Kingdom

doi 10.1136/jnnp.57.8.911

Full Text

Abstract

Available in

Date

Authors

Publisher

BMJ

Related search

Molecular Mechanism of Familial Parkinson's Disease

KAGAKU TO SEIBUTSU
2011English

Debrisoquine Oxidation Polymorphism in Patients With Rheumatoid Arthritis.

Annals of the Rheumatic Diseases
ImmunologyMolecular BiologyBiochemistryRheumatologyAllergyGenetics
1994English

Association of an Interleukin 1B Gene Polymorphism (-511) With Parkinson's Disease in Finnish Patients

Journal of Medical Genetics
Genetics
2002English

Childhood-Onset Schizophrenia and Tryptophan Hydroxylase Gene Polymorphism

American Journal of Medical Genetics
2004English

Role of Dopamine Β Hydroxylase (DBH) in Parkinson's Disease Patients of Indian Population

Molecular Cytogenetics
BiochemistryMolecular MedicineGeneticsMolecular Biology
2014English

Gene Polymorphism and Coronary Heart Disease

2012English

Association Between CD40 C/T1 Polymorphism and Familial Autoimmune Thyroid Disease

Clinical and experimental thyroidology
2013English

Relationship Between Gene Polymorphism and Plasma Dopanine .BETA.-Hydroxylase Activity in Hypertensive and Normotensive Subjects.

Hypertension Research
Internal MedicineCardiovascular MedicinePhysiologyCardiology
1994English

T313M Polymorphism of the PINK1 Gene in Parkinson’s Disease

Experimental and Therapeutic Medicine
MedicineCancer ResearchImmunologyMicrobiology
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy