Presence of val30Met and val122ile mutations in a patient...

  • Main
  • 2020 / 4
  • Presence of val30Met and val122ile mutations in a patient...
Journal of Human Genetics 2020 / 4

Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis

da Silva-Batista, Jemima A., Marques Jr, Wilson, Oliveira, Mayala Thayrine de J. S., Lins, Lucas Vergne C., Galvão, Adilson Junior P., Miguel, Diego Santana Chaves G., Machado-Costa, Marcela Câmara
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Journal:
Journal of Human Genetics
DOI:
10.1038/s10038-020-0749-3
Date:
April, 2020
File:
PDF, 498 KB
2020
Conversion to is in progress
Conversion to is failed