Bi-allelic variants in ASCC1 cause the ultrarare bone fragility disorder “spinal muscular atrophy with congenital bone fractures-2” (SMABF2). However, the mechanism by which ASCC1 dysfunction leads to
KH domains Descriptor: Defective in germ line development protein 3, isoform a Authors: Nakel, K, Hartung, S.A, Bonneau, F, Eckmann, C.R, Conti, E. Deposit date: 2010-05-28 Release date: 2010-09-22 La
PCBP2 KH1-KH2 domains Descriptor: Poly(rC)-binding protein 2 Authors: Du, Z, Fenn, S, Tjhen, R, James, T. Deposit date: 2008-01-21 Release date: 2008-08-12 Last modified: 2024-05-01 Method: SOLUTION N
Solution structure of the second KH domain in ring finger and KH domain containing protein 1 Descriptor: RING finger and KH domain-containing protein 1 Authors: Abe, C, Muto, Y, Inoue, M, Kigawa, T, T
