Homozygous mutations in the 15-hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy

Rheumatology International

Volumn 30, Issue 1, 2009, Pages 39-43

  Yüksel Konuk, Berrin ^a   SIrmacI, Asli ^a   Ayten, Gülen Ece ^b   Özdemir, Mustafa ^c   Aslan, Idil ^a   YIlmaz Turay, Ülkü ^b   Erdoǧan, Yurdanur ^b   Tekin, Mustafa ^a  

^a ANKARA UNIVERSITY   (Turkey)

^b Ataturk Chest Disease and Chest Surgery Center   (Turkey)

^c SELCUK UNIVERSITY   (Turkey)

Author keywords

15 Hydroxyprostaglandin dehydrogenase gene; Autosomal recessive; Consanguinity; Primary hypertrophic osteoarthropathy

Indexed keywords

15 HYDROXYPROSTAGLANDIN DEHYDROGENASE;

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CLUBBING FINGERS; CONSANGUINITY; CONTROLLED STUDY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SCREENING; HOMOZYGOSITY; HUMAN; MALE; OSTEOARTHROPATHY; PHENOTYPE; PRIORITY JOURNAL; TURKEY (REPUBLIC);

ADOLESCENT; ADULT; BASE SEQUENCE; CASE-CONTROL STUDIES; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEREDITY; HOMOZYGOTE; HUMANS; HYDROXYPROSTAGLANDIN DEHYDROGENASES; MALE; MOLECULAR SEQUENCE DATA; MUTATION; OSTEOARTHROPATHY, PRIMARY HYPERTROPHIC; PEDIGREE; PHENOTYPE; TURKEY; YOUNG ADULT;

EID: 71349084135     PISSN: 01728172     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00296-009-0895-6     Document Type: Article

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