Author :

Name  Zabel B
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4 Publications

First Author Title Year Journal Volume Pages
Rodriguez P Functional characterization of human nucleosome assembly protein-2 (NAP1L4) suggests a role as a histone chaperone. 1997 Genomics 44 253-65
Gedeon AK The molecular basis of X-linked spondyloepiphyseal dysplasia tarda. 2001 Am J Hum Genet 68 1386-97
Hermanns P Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis. 2008 Am J Hum Genet 82 1368-74
Unger S Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations. 2008 Nat Genet 40 287-9



To cite PlanMine, please refer to the following publication:

Rozanski, A., Moon, H., Brandl, H., Martín-Durán, J. M., Grohme, M., Hüttner, K., Bartscherer, K., Henry, I., & Rink, J. C.
PlanMine 3.0—improvements to a mineable resource of flatworm biology and biodiversity
Nucleic Acids Research, gky1070. doi:10.1093/nar/gky1070 (2018)