首页> 外文OA文献 >A third MRX family (MRX68) is due to mutation in the Long-Chain Fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients.

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A third MRX family (MRX68) is due to mutation in the Long-Chain Fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients.

机译：第三个mRX家族（mRX68）是长链脂肪酸-Coa连接酶4（FaCL4）基因中的两个突变：用于筛选智障患者的快速酶测定的提议。

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LONGO I; FRINTS S; FRYNS JP; MELONI I; PESCUCCI C; ARIANI F; BORGHGRAEF M; RAYNAUD M; MARYNEN P; SCHWARTZ C; A. RENIERI; AND FROYEN G;
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年度 2003
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1. A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients. [J] . Longo I, Frints SG, Fryns JP, Journal of Medical Genetics . 2003,第1期

机译：第三个MRX家族（MRX68）是长链脂肪酸CoA连接酶4（FACL4）基因突变的结果：一种用于筛查弱智患者的快速酶法测定的建议。
2. No association between polymorphisms in the FACL4 (fatty acid-CoA ligase 4) gene and nonspecific mental retardation in Qin-Ba mountain region of China. [J] . An C, Gao X, Shi Z, Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences . 2008,第2期

机译：中国秦巴山区FACL4（脂肪酸-CoA连接酶4）基因的多态性与非特异性智力障碍之间没有关联。
3. FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. [J] . Meloni I, Muscettola M, Raynaud M, Nature Genetics . 2002,第4期

机译：编码脂肪酸CoA连接酶4的FACL4突变为非特异性X连锁智力低下。
4. A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients [O] . I Longo, S Frints, J Fryns, 2003

机译：第三个MRX家族（MRX68）是长链脂肪酸CoA连接酶4（FACL4）基因突变的结果：一种用于筛查弱智患者的快速酶法测定的建议
5. A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients [O] . Longo, I, Frints, S G M, Fryns, Jean-Pierre, 2003

机译：第三个MRX家族（MRX68）是长链脂肪酸CoA连接酶4（FACL4）基因突变的结果：一种用于筛查弱智患者的快速酶法测定的建议

A third MRX family (MRX68) is due to mutation in the Long-Chain Fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients.

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