Association of the insertion/deletion polymorphism of the angiotensin I-converting enzyme gene in patients of migraine with aura
- 10 February 2005
- journal article
- research article
- Published by Elsevier in Neuroscience Letters
- Vol. 374 (2) , 129-131
- https://doi.org/10.1016/j.neulet.2004.10.041
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2Nature Genetics, 2003
- Angiotensin-Converting Enzyme Gene Deletion Polymorphism Determines an Increase in Frequency of Migraine Attacks in Patients Suffering from Migraine without AuraEuropean Neurology, 2000
- Mistyping frequency of the angiotensin-converting enzyme gene polymorphism and an improved method for its avoidanceHuman Genetics, 1997
- An insertion/deletion polymorphism in the angiotensin converting enzyme gene is associated with both brain substance P contents and affective disordersBiological Psychiatry, 1996
- Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4Cell, 1996
- Migraine Without Aura and Migraine with Aura are Inherited DisordersCephalalgia, 1996
- ACE Inhibitors for Prophylaxis of Migraine HeadachesHeadache: The Journal of Head and Face Pain, 1995
- Angiotensin-Converting Enzyme Gene Deletion PolymorphismStroke, 1995
- PCR detection of the insertion/deletion polymorphism of the human angiotensin converting enzyme gene (DCP1) (dipeptidyl carboxypeptidase 1)Nucleic Acids Research, 1992
- An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels.Journal of Clinical Investigation, 1990