Skip to content

Opening book details…

About this Biochemistry, Genetics and Molecular Biology article

MYH1 is a candidate gene for recurrent rhabdomyolysis in humans by Alsaif, Hessa S. (author);Alshehri, Ali (author);Sulaiman, Raashda A. (author);Al‐Hindi, Hindi (author);Guzmán‐Vega, Francisco J. (author);Arold, Stefan T. (author);Alkuraya, Fowzan S. (author) 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
Alsaif, Hessa S. (author);Alshehri, Ali (author);Sulaiman, Raashda A. (author);Al‐Hindi, Hindi (author);Guzmán‐Vega, Francisco J. (author);Arold, Stefan T. (author);Alkuraya, Fowzan S. (author)
Publisher
Wiley
Published
2021
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

More by Alsaif, Hessa S. (author);Alshehri, Ali (author);Sulaiman, Raashda A. (author);Al‐Hindi, Hindi (author);Guzmán‐Vega, Francisco J. (author);Arold, Stefan T. (author);Alkuraya, Fowzan S. (author)

Browse all works by Alsaif, Hessa S. (author);Alshehri, Ali (author);Sulaiman, Raashda A. (author);Al‐Hindi, Hindi (author);Guzmán‐Vega, Francisco J. (author);Arold, Stefan T. (author);Alkuraya, Fowzan S. (author)