SCOPUS 정보 검색 플랫폼

Volumn 71, Issue 3, 2002, Pages 656-662

Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype

(13) Paloneva, Juha a Manninen, Tuula b Christman, Grant b Hovanes, Karine b Mandelin, Jami a Adolfsson, Rolf c Bianchin, Marino d Bird, Thomas e Miranda, Roxana f Salmaggi, Andrea g Tranebjærg, Lisbeth h,i Konttinen, Yrjö a Peltonen, Leena a,b

a HELSINKI UNIVERSITY CENTRAL HOSPITAL (Finland)

b UNIVERSITY OF CALIFORNIA (United States)

c UMEÅ UNIVERSITY (Sweden)

d Hospital Regional de São Josç (Brazil)

e VETERANS AFFAIRS MEDICAL CENTER (United States)

f Department of Internal Medicine (Bolivia)

g DEPARTMENT OF NEUROSURGERY (Italy)

h UNIVERSITY HOSPITAL OF NORTH NORWAY (Norway)

i BISPEBJERG HOSPITAL (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE RECEPTOR; RECEPTOR SUBUNIT;

ARTICLE; BONE CYST; BONE DYSPLASIA; BONE MARROW CELL; CELLULAR IMMUNITY; DEMENTIA; DENDRITIC CELL; DISEASE COURSE; GENE; GENE MUTATION; GENETIC CODE; HUMAN; IMMUNE RESPONSE; LEUKOENCEPHALOPATHY; MACROPHAGE; MOLECULAR GENETICS; NASUHAKOLA DISEASE; NATURAL KILLER CELL; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA; PRIORITY JOURNAL; RECEPTOR GENE; RECESSIVE INHERITANCE; SCLEROSING LEUKOENCEPHALOPATHY; SIGNAL TRANSDUCTION; TYROBP GENE;

EID: 18544390923 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1086/342259 Document Type: Article

Times cited : (542)

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