SCOPUS 정보 검색 플랫폼

Volumn 92, Issue 7, 2013, Pages 1003-1004

Alu repeat-induced deletions in chronic granulomatous disease: A cause not only for p67-phox, but also for p47-phox deficiency

(6) Winkler, Stefan a Van Leeuwen, Karin b Deboer, Martin b Rösen Wolff, Angela a Roos, Dirk b Roesler, Joachim a

a UNIVERSITY HOSPITAL CARL GUSTAV CARUS (Germany)

b UNIVERSITY OF AMSTERDAM (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; PROTEIN P67; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE;

ALU REPEAT; AUTOSOMAL RECESSIVE DISORDER; CHRONIC GRANULOMATOUS DISEASE; DNA DETERMINATION; DNA STRUCTURE; ENZYME DEFICIENCY; ENZYME SUBUNIT; EXON; GENE; GENE CONVERSION; GENE DELETION; GENETIC RECOMBINATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; LETTER; NCF1 GENE; NCF2 GENE; PRIORITY JOURNAL; PSEUDOGENE;

ALU ELEMENTS; GRANULOMATOUS DISEASE, CHRONIC; HUMANS; NADPH OXIDASE; PHOSPHOPROTEINS; SEQUENCE DELETION;

EID: 84878957781 PISSN: 09395555 EISSN: 14320584 Source Type: Journal
DOI: 10.1007/s00277-012-1661-5 Document Type: Letter

Times cited : (4)

References (4)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.