Paper Details

Paper Title

X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.

Paper Journal Title

Nat Genet

Paper Citation Count

314

Paper Publication Year

2008

Bio Mention

737, EFMR, Epilepsy and mental retardation, PCDH19, PCDH19 mRNA, X chromosome, X chromosome genes, X-linked protocadherin 19, cadherin superfamily, calcium, cognitive impairment, epilepsy, female-limited epilepsy, human, mental retardation, mouse, premature termination codon, protocadherin 19, protocadherin 19 (PCDH19) gene

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