SCOPUS 정보 검색 플랫폼

Neurogenetics

Volumn 11, Issue 3, 2010, Pages 367-368

Questionable association between a monoamine oxidase a promoter polymorphism and sudden infant death syndrome

(2) Klintschar, Michael a Heimbold, Christian b

a HANNOVER MEDICAL SCHOOL (Germany)

b UNIVERSITY OF GÖTTINGEN (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING);

ALLELE; CHROMOSOMAL LOCALIZATION; CONTROLLED STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC TRANSCRIPTION; HUMAN; INFANT; LETTER; MALE; PRIORITY JOURNAL; STILLBIRTH; SUDDEN INFANT DEATH SYNDROME; X CHROMOSOME; GENETICS; NEWBORN; PROMOTER REGION; X CHROMOSOMAL INHERITANCE;

FEMALE; GENES, X-LINKED; GENETIC ASSOCIATION STUDIES; HUMANS; INFANT, NEWBORN; MALE; MONOAMINE OXIDASE; POLYMORPHISM, GENETIC; PROMOTER REGIONS, GENETIC; SUDDEN INFANT DEATH;

EID: 77954658088 PISSN: 13646745 EISSN: None Source Type: Journal
DOI: 10.1007/s10048-010-0242-9 Document Type: Letter

Times cited : (9)

References (5)

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2
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- Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome
- Nonnis Marzano F, Maldini M, Filonzi L, Lavezzi AM, Parmigiani S, Magnani C, Bevilacqua G, Matturri L (2008) Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome. Genomics 91(6):485-491
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3
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- Impact of sodium/proton exchanger 3 gene variants on sudden infant death syndrome
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4
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- A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome
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- Klintschar M, Reichenpfader B (2008) Saternus KS (2008) A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome. J Pediatr 153(2):190-193
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5
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- The X-linkage hypotheses for SIDS and the male excess in infant mortality
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.