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Leukemia Research

Volumn 33, Issue 9, 2009, Pages

Disease causing nature of homozygous missense, p.A523D, alteration in the perforin gene

(7) Oner, Ahmet Faik a Okur, Hamza b Balta, Gunay b Unal, Sule b Deger, Ibrahim a Akarsu, Nurten b Gurgey, Aytemiz b

a YUZUNCU YIL UNIVERSITY (Turkey)

b HACETTEPE UNIVERSITY (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

PERFORIN;

AMINO ACID SUBSTITUTION; BONE MARROW EXAMINATION; CLINICAL FEATURE; FAMILY HISTORY; GENE FREQUENCY; GENETIC ANALYSIS; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; LETTER; MISSENSE MUTATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

CHILD; FEMALE; HOMOZYGOTE; HUMANS; MUTATION, MISSENSE; PERFORIN;

EID: 67549094643 PISSN: 01452126 EISSN: None Source Type: Journal
DOI: 10.1016/j.leukres.2009.03.041 Document Type: Letter

Times cited : (2)

References (5)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.