Authors:
Nurnberg, P
Thiele, H
Chandler, D
Hohne, W
Cunningham, ML
Ritter, H
Leschik, G
Uhlmann, K
Mischung, C
Harrop, K
Goldblatt, J
Borochowitz, ZU
Kotzot, D
Westermann, F
Mundlos, S
Braun, HS
Laing, N
Tinschert, S
Citation: P. Nurnberg et al., Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia, NAT GENET, 28(1), 2001, pp. 37-41