A Novel Mutation H373Y in the Wilms’ Tumor Suppressor Gene, WT1 Associated with Denys-Drash Syndrome
Copyright policy ) M, Ghahremani; C B, Chan; T, Bistritzer; M M, Aladjem; M, Tieder; J, Pelletier;
A Novel Mutation H373Y in the Wilms’ Tumor Suppressor Gene, WT1 Associated with Denys-Drash Syndrome
- McGill University Canada
- Assaf Harofeh Medical Center Israel
Male, Genes, Wilms Tumor, Nephrotic Syndrome, Child, Preschool, Disorders of Sex Development, Humans, Point Mutation, Tyrosine, Histidine, Polymerase Chain Reaction, Polymorphism, Single-Stranded Conformational
Male, Genes, Wilms Tumor, Nephrotic Syndrome, Child, Preschool, Disorders of Sex Development, Humans, Point Mutation, Tyrosine, Histidine, Polymerase Chain Reaction, Polymorphism, Single-Stranded Conformational
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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).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
Popularity provided by BIP! 1
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