1 – 1 of 1
- show: 50
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2019
-
Mark
Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene
(
- Contribution to journal › Letter