T/G polymorphism at intron 9 of presenilin 1 gene is associated with, but not responsible for sporadic late-onset Alzheimer's disease in Japanese population

Neuroscience Letters

Volumn 227, Issue 2, 1997, Pages 123-126

  Nishiwaki, Yumiko ^a   Kamino, Kouzin ^a   Yoshiiwa, Aoi ^a   Sato, Naoyuki ^a   Tateishi, Kyoko ^a   Takeda, Masatoshi ^a   Kobayashi, Toshiko ^b   Yamamoto, Hideki ^b   Nonomura, Yasuhiro ^c   Yoneda, Hiroshi ^c   Sakai, Toshiaki ^c   Imagawa, Masaki ^d   Miki, Tetsuro ^a   Ogihara, Toshio ^a  

^a OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

^b Osaka Municipal Kohsaiin Hospital   (Japan)

^c OSAKA MEDICAL COLLEGE   (Japan)

^d HYOGO PREFECTURAL AMAGASAKI GENERAL MEDICAL CENTER   (Japan)

Author keywords

Alzheimer's disease; D14S43; FOS; Genetics; Population variation; Presenilin 1

Indexed keywords

ADULT; AGED; ALLELE; ALZHEIMER DISEASE; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENETIC POLYMORPHISM; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; POPULATION GENETICS; PRIORITY JOURNAL;

AGE OF ONSET; AGED; AGED, 80 AND OVER; ALZHEIMER DISEASE; FEMALE; HUMANS; INTRONS; JAPAN; MALE; MEMBRANE PROTEINS; POLYMORPHISM, GENETIC; PRESENILIN-1;

EID: 0030973408     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3940(97)00317-0     Document Type: Article

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