American Journal of Medical Genetics Part A
Article . 2015 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
CNKSR2 deletions: A novel cause of X‐linked intellectual disability and seizures
Authors: Umut, Aypar; Elaine C, Wirrell; Nicole L, Hoppman;
doi: 10.1002/ajmg.a.36902
pmid: 25754917
CNKSR2 deletions: A novel cause of X‐linked intellectual disability and seizures
Related Organizations
- Mayo Clinic United States
Keywords
Male, Chromosomes, Human, X, X-Linked Intellectual Disability, Humans, Child, Microarray Analysis, Gene Deletion, Adaptor Proteins, Signal Transducing
Male, Chromosomes, Human, X, X-Linked Intellectual Disability, Humans, Child, Microarray Analysis, Gene Deletion, Adaptor Proteins, Signal Transducing
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citations
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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
Popularity 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.
26
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