UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly
- 26 May 2021
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 23 (9), 1624-1635
- https://doi.org/10.1038/s41436-021-01182-1
Abstract
No abstract availableThis publication has 33 references indexed in Scilit:
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