Lack of Association between an Intronic Polymorphism in the Presenilin-1 Gene and Sporadic Late-Onset Alzheimer Disease in Polish Patients

Publisher： Karger

E-ISSN： 1421-9824|9|3|137-139

ISSN： 1420-8008

Source： Dementia and Geriatric Cognitive Disorders, Vol.9, Iss.3, 1998-04, pp. : 137-139

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Association Study of Cathepsin D Gene Polymorphism in Iranian Patients with Sporadic Late-Onset Alzheimer's Disease

By  

Dementia and Geriatric Cognitive Disorders, Vol. 37, Iss. 5-6, 2013-11 ,pp. : 257-264

Karger

Access to resources Recommend Favorite

F175S Change and a Novel Polymorphism in Presenilin-1 Gene in Late-Onset Familial Alzheimer’s Disease

By  

European Neurology, Vol. 47, Iss. 4, 2002-05 ,pp. : 209-213

Karger

Access to resources Recommend Favorite

Association between Glycogen Synthase Kinase-3β Genetic Polymorphism and Late-Onset Alzheimer’s Disease

By  

Dementia and Geriatric Cognitive Disorders, Vol. 21, Iss. 4, 2006-04 ,pp. : 228-232

Karger

Access to resources Recommend Favorite

Interleukin-1α –889 C/T Polymorphism in Turkish Patients with Late-Onset Alzheimer’s Disease

By  

Dementia and Geriatric Cognitive Disorders, Vol. 27, Iss. 1, 2009-01 ,pp. : 82-87

Karger

Access to resources Recommend Favorite

Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease

By  

Medical Principles and Practice, Vol. 24, Iss. 4, 2015-05 ,pp. : 351-354

Karger

Access to resources Recommend Favorite