Publication not explained
This publication has not yet been explained in plain language by the author(s). However, you can still read the publication.
If you are one of the authors, claim this publication so you can create a plain language summary to help more people find, understand and use it.
Featured Image
Read the Original
This page is a summary of: Coexistence of mutations in keratin 10 (KRT10) and the mitochondrial genome in a patient with ichthyosis with confetti and Leber's hereditary optic neuropathy, American Journal of Medical Genetics Part A, September 2017, Wiley,
DOI: 10.1002/ajmg.a.38403.
You can read the full text:
Contributors
The following have contributed to this page