Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia Journal Articles Refereed uri icon

Overview

Authors

  • Authorship

    • OATES C
    • FOLEY A
    • HURLES
    • HOULDEN
    • GREENSMITH
    • AUER-GRUMBACH
    • PIEBER R
    • STROM M
    • SCHULE
    • HERRMANN N
    • SOWDEN E
    • ROSSOR M
    • ACSADI
    • MENEZES P
    • CLARKE F
    • ZUCHNER
    • MUNTONI
    • PROF Kathryn North
    • REILLY M
    • HAFEZPARAST
    • GONZALEZ
    • SPEZIANI
    • MACARTHUR G
    • LEK
    • COTTENIE
    • SCOTO

Published in

  • American Journal of Human Genetics

Time

Date/time value

  • 2013

Identity

Digital Object Identifier (DOI)

  • 10.1016/j.ajhg.2013.04.018

Additional Document Info

Parent Title

  • American Journal of Human Genetics

Volume

  • 92

Issue

  • 6

Publisher

  • University of Chicago Press