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About this Biochemistry, Genetics and Molecular Biology article
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement by Gonzalez-Quereda, Lidia; Gallardo, Eduard; Töpf, Ana; Alonso-Jimenez, Alicia; Straub, Volker; Rodriguez, Maria Jose; Lleixa, Cinta; Illa, Isabel; Gallano, Pia; Diaz-Manera, Jordi is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Gonzalez-Quereda, Lidia; Gallardo, Eduard; Töpf, Ana; Alonso-Jimenez, Alicia; Straub, Volker; Rodriguez, Maria Jose; Lleixa, Cinta; Illa, Isabel; Gallano, Pia; Diaz-Manera, Jordi
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0960-8966)
- Published
- 2018
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)