A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys— Drash syndrome
Authors: O, Ogawa; M R, Eccles; K, Yun; R F, Mueller; M D, Holdaway; A E, Reeve;
doi: 10.1093/hmg/2.2.203
pmid: 8098976
A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys— Drash syndrome
Related Organizations
- University of Otago New Zealand
Keywords
Male, Hypospadias, Genes, Wilms Tumor, Base Sequence, DNA Mutational Analysis, Molecular Sequence Data, Disorders of Sex Development, Zinc Fingers, Syndrome, Wilms Tumor, Kidney Neoplasms, Mutagenesis, Insertional, Cryptorchidism, Humans, Kidney Failure, Chronic, Amino Acid Sequence, Child
Male, Hypospadias, Genes, Wilms Tumor, Base Sequence, DNA Mutational Analysis, Molecular Sequence Data, Disorders of Sex Development, Zinc Fingers, Syndrome, Wilms Tumor, Kidney Neoplasms, Mutagenesis, Insertional, Cryptorchidism, Humans, Kidney Failure, Chronic, Amino Acid Sequence, Child
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
popularity
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This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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