Publication | Open Access
UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly
18
Citations
24
References
2021
Year
Uba2 VariantsDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsPathogenesisPathologyMolecular GeneticsRecognizable SyndromeDisease Gene IdentificationMedicine
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