@dpavot:29666464 / 28-33
|
We report a case with novel AARS2 gene mutations with developed striking cerebellar atrophy and leukoencephalopathy, which helps to further understand the clinical and genetic heterogeneity of AARS2-L.
|
projects
| Unselected / annnotation | Selected / annnotation | |
|
|
|
|