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Long-Term Clinical Profile of Children With the Low-Penetrance R92Q Mutation of the TNFRSF1A Gene

机译：TNFRSF1A基因低渗透性R92Q突变儿童的长期临床概况

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Pelagatti, M A; Meini, A; Caorsi, R; Cattalini, M; Federici, S; Zulian, F; Calcagno, G; Tommasini, A; Bossi, G; Sormani, M P; Caroli, F; Plebani, A; Ceccherini, I; Martini, A; Gattorno, M;
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年度 2011
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正文语种 {"code":"en","name":"English","id":9}
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1. 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
2. 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。
3. 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
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. The effect of mutations in stearoyl CoA desaturase gene and fatty acid synthase on milk composition and fatty acid profile in milk fat of dairy cows. [D] . Clark, Laura Ashley. 2009

机译：硬脂酰辅酶A去饱和酶基因和脂肪酸合酶突变对奶牛乳汁组成和脂肪酸谱的影响。
6. Long-Term Clinical Profile of Children With the Low-Penetrance R92Q Mutation of the TNFRSF1A Gene [O] . M A Pelagatti, A Meini, R Caorsi, -1

机译：TNFRSF1A基因低渗透性R92Q突变儿童的长期临床概况
7. Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene. [O] . Pelagatti MA, Meini A, Caorsi R, 2011

机译：TNFRSF1A基因低渗透性R92Q突变患儿的长期临床资料。

Long-Term Clinical Profile of Children With the Low-Penetrance R92Q Mutation of the TNFRSF1A Gene

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