Showing results 1 to 2 of 2
| Title | Author(s) | Issue Date | |
|---|---|---|---|
| 2021 | |||
The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes Journal:Molecular Genetics & Genomic Medicine | 2020 |