Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics,Molecular Biology
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Toxicoproteomic assessment of liver responses to acute pyrrolizidine alkaloid intoxication in rats;Journal of Environmental Science and Health, Part C;2018-04-03
2. Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous mutation in ACTA1 (Asp154Asn);Acta Neuropathologica;2004-06-24
3. Inherited disorders of sarcomeric proteins;Current Opinion in Neurology;1999-10
4. Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy;Nature Genetics;1999-10
5. Physical Mapping of the Rippling Muscle Disease Locus;Genomics;1999-02
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