Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series. Other Refereed Contribution to Refereed Journals uri icon

Overview

Authors

  • Authorship

    • REVAH-POLITI A
    • DR Slave Petrovski
    • WILSON AL
    • AGGARWAL VS
    • ANYANE-YEBOA K
    • GANAPATHI M
    • BIER L
    • CHO MT
    • GOLDSTEIN DB
    • HEMATI P
    • IGLESIAS A
    • JUUSOLA J
    • PAPPAS J

Published in

  • American Journal of Medical Genetics. Part A

Time

Date/time value

  • 2017

Identity

Digital Object Identifier (DOI)

  • 10.1002/ajmg.a.38460

Additional Document Info

Parent Title

  • Am J Med Genet A

Volume

  • 173

Issue

  • 12

Publisher

  • John Wiley & Sons