학술논문
UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly
Document Type
Article
Author
Schnur, R.E.; Rhodes, L.; Sacoto, M.J.G.; Wentzensen, I.M.; Juusola, J.; Scarano, M.I.; Yousaf, S.; Liu, J.; Flage, M.; Kuppa, S.; Navarro, K.; Hufnagel, R.B.; Chung, W.K.; Marble, M.; Zambrano, R.M.; Sobreira, N.; Jayakar, P.; Pierpont, M.E.; Schultz, M.J.; Pichurin, P.N.; Olson, R.J.; Graham, G.E.; Osmond, M.; Contreras-García, G.A.; Campo-Neira, K.A.; Peñaloza-Mantilla, C.A.; Prada, C.E.
Source
In: Genetics in Medicine . (Genetics in Medicine, September 2021, 23(9):1624-1635)
Subject
Language
English
ISSN
15300366
10983600
10983600