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Schema
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Person
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Entries
Jackson, CE
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created
[InstanceEdit:2314587] Jassal, B, 2012-06-07
dbId
2314575
displayName
Jackson, CE
firstname
C E
initial
CE
publications
[LiteratureReference:2314582] Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneity
[LiteratureReference:8853604] Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B
[LiteratureReference:8858635] Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
[LiteratureReference:8858617] Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
schemaClass
Person
surname
Jackson
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