학술논문
Further clinical and molecular characterization of an XLID syndrome associated with BRWD3 variants, a gene implicated in the leukemia-related JAK-STAT pathway
Document Type
Article
Author
Delanne, J.; Thauvin-Robinet, C.; Lecat, M.; Pöe, C.; Chevarin, M.; Garde, A.; Thomas, Q.; Faivre, L.; Jouan, T.; Tisserant, E.; Duffourd, Y.; Philippe, C.; Kuentz, P.; Blackburn, P.R.; Klee, E.W.; Stumpel, C.T.R.M.; Stegmann, S.; Stevens, S.J.C.; Nava, C.; Heron, D.; Keren, B.; Mahida, S.; Naidu, S.; Babovic-Vuksanovic, D.; Herkert, J.C.; Torring, P.M.; Ousager, L.B.; Kibæk, M.; De Bie, I.; Pfundt, R.; Hendriks, Y.M.C.; Bend, R.; Warren, H.; Skinner, S.A.; Lyons, M.J.
Source
In: European Journal of Medical Genetics . (European Journal of Medical Genetics, January 2023, 66(1))
Subject
Language
English
ISSN
18780849
17697212
17697212