Fibrillin-1 gene analysis of Korean patients with spontaneous CSF hypovolemia

Headache

Volumn 47, Issue 1, 2007, Pages 111-115

  Chung, Sun J ^a   Ki, Chang Seok ^b   Lee, Myoung C ^a   Lee, Jae Hong ^a,c  

^a University of Ulsan   (South Korea)

^b Sungkyunkwan University   (South Korea)

^c Asan Medical Center   (South Korea)

Author keywords

CSF hypovolemia; Fibrillin 1 (FBN1) gene; Marfan's syndrome

Indexed keywords

FIBRILLIN 1;

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIABILITY; HUMAN; HYPOVOLEMIA; INTRON; KOREA; MALE; MARFAN SYNDROME; POPULATION RESEARCH; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SPONTANEOUS CEREBROSPINAL FLUID HYPOVOLEMIA;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CEREBROSPINAL FLUID; CEREBROSPINAL FLUID PRESSURE; FEMALE; HUMANS; INTRACRANIAL HYPOTENSION; KOREA; MALE; MARFAN SYNDROME; MICROFILAMENT PROTEINS; MIDDLE AGED; MUTATION; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 33846259753     PISSN: 00178748     EISSN: 15264610     Source Type: Journal    
DOI: 10.1111/j.1526-4610.2006.00635.x     Document Type: Article

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