首页> 外文OA文献 >PReS-FINAL-2235: Overlap of homozygous TNFRSF1A R92Q mutation with MEVF E148Q mutation versus homozygous TNFRSF1A R92Q mutation: difference in clinical profile in two sisters from Oman

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PReS-FINAL-2235: Overlap of homozygous TNFRSF1A R92Q mutation with MEVF E148Q mutation versus homozygous TNFRSF1A R92Q mutation: difference in clinical profile in two sisters from Oman

机译：PReS-FINAL-2235：具有MEVF E148Q突变的纯合TNFRSF1A R92Q突变与纯合TNFRSF1A R92Q突变的重叠：阿曼的两个姐妹的临床特征差异

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1. PReS-FINAL-2235: Overlap of homozygous TNFRSF1A R92Q mutation with MEVF E148Q mutation versus homozygous TNFRSF1A R92Q mutation: difference in clinical profile in two sisters from Oman [J] . R Abdwani, S Abrawi, E Ibraheem, Pediatric rheumatology online journal . 2013,第S2期

机译：PReS-FINAL-2235：带有MEVF E148Q突变的纯合TNFRSF1A R92Q突变与纯合TNFRSF1A R92Q突变的重叠：阿曼的两个姐妹的临床特征差异
2. Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene? [J] . M. A. Pelagatti, A. Meini, R. Caorsi, Arthritis & Rheumatism . 2011,第4期

机译：TNFRSF1A基因？的低渗透性R92Q突变患儿的长期临床特征
3. Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene. [J] . Pelagatti MA, Meini A, Caorsi R, Arthritis and Rheumatism . 2011,第4期

机译：TNFRSF1A基因低渗透性R92Q突变患儿的长期临床资料。
4. TNFRSF1A MUTATIONS IN ITALIAN PATIENTS AFFECTED BY APPARENTLY SPORADIC PERIODIC FEVER SYNDROME [C] . L Obici, S. Marciano, G. Palladini, International Symposium on Amyloidosis . 2005

机译：受明显散发性周期性发烧综合征影响的意大利患者的TNFRSF1A突变
5. Homozygous protein C deficiency: identification of a novel missense mutation that causes impaired secretion of the mutant protein C [D] . Yamamoto Koji, Matsushita Tadashi, Sugiura Isamu, 1992

机译：纯合蛋白C缺乏症：鉴定导致突变蛋白C分泌受损的新型错义突变
6. PReS-FINAL-2235: Overlap of homozygous TNFRSF1A R92Q mutation with MEVF E148Q mutation versus homozygous TNFRSF1A R92Q mutation: difference in clinical profile in two sisters from Oman [O] . R Abdwani, S Abrawi, E Ibraheem, 2013

机译：PReS-FINAL-2235：具有MEVF E148Q突变的纯合TNFRSF1A R92Q突变与纯合TNFRSF1A R92Q突变的重叠：阿曼的两个姐妹的临床特征差异
7. Long-Term Clinical Profile of Children With the Low-Penetrance R92Q Mutation of the TNFRSF1A Gene [O] . Pelagatti, M A, Meini, A, Caorsi, R, 2011

机译：TNFRSF1A基因低渗透性R92Q突变儿童的长期临床概况

PReS-FINAL-2235: Overlap of homozygous TNFRSF1A R92Q mutation with MEVF E148Q mutation versus homozygous TNFRSF1A R92Q mutation: difference in clinical profile in two sisters from Oman

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