학술논문
Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms
Document Type
Article
Author
Yabumoto, M.; Singh, M.; Palafox, M.F.; Krakow, D.; Arboleda, V.A.; Wei, A.; Elliott, K.; Kianmahd, J.; Schweitzer, D.N.; Goodloe, D.H.; Dean, S.J.; Gooch, C.; Murray, B.K.; Swartz, E.; Schrier Vergano, S.A.; Towne, M.C.; Nugent, K.; Roeder, E.R.; Kresge, C.; Pletcher, B.A.; Grand, K.; Graham, J.M.; Gates, R.; Gomez-Ospina, N.; Ramanathan, S.; Clark, R.D.; Glaser, K.; Benke, P.J.; Cohen, J.S.; Fatemi, A.; Baranano, K.W.; Mu, W.; Madden, J.A.; Gubbels, C.S.; Yu, T.W.; Agrawal, P.B.; O’Donnell-Luria, A.; Chambers, M.-K.; Phornphutkul, C.; Pugh, J.A.; Tauber, K.A.; Azova, S.; Smith, J.R.; Medsker, H.; Srivastava, S.
Source
In: Molecular Genetics and Genomic Medicine . (Molecular Genetics and Genomic Medicine, October 2021, 9(10))
Subject
Language
English
ISSN
23249269