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Association of a mutation in LACC1 with a monogenic form of systemic juvenile idiopathic arthritis.
Wakil, Salma M; Monies, Dorota M; Abouelhoda, Mohamed; Al-Tassan, Nada; Al-Dusery, Haya; Naim, Ewa A; Al-Younes, Banan; Shinwari, Jameela; Al-Mohanna, Futwan A; Meyer, Brian F; Al-Mayouf, Sulaiman.
Affiliation
  • Wakil SM; King Faisal Specialist Hospital and Research Centre, and King Abdulaziz City for Science and Technology, Riyadh, Saudi Arabia.
Arthritis Rheumatol ; 67(1): 288-95, 2015 Jan.
Article in En | MEDLINE | ID: mdl-25220867
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arthritis, Juvenile / Mutation, Missense / Laccase / Genetic Linkage Type of study: Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Arthritis Rheumatol Year: 2015 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arthritis, Juvenile / Mutation, Missense / Laccase / Genetic Linkage Type of study: Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Country/Region as subject: Asia Language: En Journal: Arthritis Rheumatol Year: 2015 Document type: Article Affiliation country: