Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency Journal Articles Refereed uri icon

Overview

Authors

  • Authorship

    • TAN C
    • KUMAR R
    • DOUGLAS E
    • NGUYEN LS
    • MCMAHON J
    • SADLEIR L
    • SPECCHIO N
    • MARINI C
    • GUERRINI R
    • MOLLER RS
    • DEPIENNE C
    • SHARD C
    • HAAN E
    • THOMAS PQ
    • PROF Sam Berkovic
    • PROF Ingrid Scheffer
    • GECZ J
    • RANIERI E
    • HYNES K
    • PHAM DH
    • LEACH D
    • BUCHANAN G
    • CORBETT M
    • SHOUBRIDGE C

Published in

  • Human Molecular Genetics

Time

Date/time value

  • 2015

Identity

Digital Object Identifier (DOI)

  • 10.1093/hmg/ddv245

Additional Document Info

Parent Title

  • HUMAN MOLECULAR GENETICS

Volume

  • 24

Issue

  • 18

Publisher

  • Oxford University Press