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Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2.

机译：对瑞士牛的Weaver综合征进行精细定位，并鉴定NRCam，pNpLa8和CTTNBp2中的41个一致突变。

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Matthew McClure; Euisoo Kim; Derek Bickhart; Daniel Null; Tabatha Cooper; John Cole; George Wiggans; Paolo Ajmone-Marsan; Licia Colli; Enrico Santus; George E Liu; Steve Schroeder; Lakshmi Matukumalli; Curt Van Tassell; Tad Sonstegard;
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1. Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle [J] . Elisabeth Kunz, Sophie Rothammer, Hubert Pausch, Genetics, selection, evolution . 2016 ,第1期

机译：确认PNPLA8中的非同义SNP是布朗瑞士牛Weaver综合征的候选因果突变
2. Bovine Progressive Degenerative Myeloencephalopathy (Weaver Syndrome) in Brown Swiss Cattle in Canada: A Literature Review and Case Report [J] . John D. Baird, Ulla M. Sarmiento, Parvathi K. Basrur The Canadian veterinary journal . 1988 ,第4期

机译：加拿大布朗瑞士牛的牛进行性退行性脊髓性脑病（Weaver综合征）：文献复习和病例报告
3. Quantitative trait loci mapping for conjugated linoleic acid, vaccenic acid and Delta(9)-desaturase in Italian Brown Swiss dairy cattle using selective DNA pooling [J] . Strillacci MG, Frigo E, Canavesi F, Animal Genetics . 2014 ,第4期

机译：使用选择性DNA池分析意大利棕色瑞士奶牛中共轭亚油酸，痘苗酸和Delta（9）-去饱和酶的定量性状基因座
4. Neuromuscular studies in Brown Swiss cattle affected with bovine progressive degenerative myeloencephalopathy (Weaver syndrome). [D] . Oyster, Ronald Alan. 1991

机译：对患有牛进行性退行性脊髓性脑病（Weaver综合征）的棕色瑞士牛的神经肌肉研究。
5. Fine Mapping for Weaver Syndrome in Brown Swiss Cattle and the Identification of 41 Concordant Mutations across NRCAM PNPLA8 and CTTNBP2 [O] . Matthew McClure, Euisoo Kim, Derek Bickhart, -1

机译：精细定位韦弗综合征瑞士褐牛和41个谐和突变的整个NRCampNpLa8和CTTNBp2鉴定
6. Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle [O] . Elisabeth Kunz, Sophie Rothammer, Hubert Pausch, 2016

机译：确认PNPLA8中的非同义SNP是布朗瑞士牛Weaver综合征的候选因果突变

Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2.

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