Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly Journal Article uri icon

Overview

publication date

  • January 1, 2010

has restriction

  • bronze

Date in CU Experts

  • February 8, 2019 4:32 AM

Full Author List

  • Schaefer E; Zaloszyc A; Lauer J; Durand M; Stutzmann F; Perdomo-Trujillo Y; Redin C; Greene VB; Toutain A; Perrin L

author count

  • 24

citation count

  • 64

Other Profiles

International Standard Serial Number (ISSN)

  • 1661-8769

Electronic International Standard Serial Number (EISSN)

  • 1661-8777

Additional Document Info

start page

  • 273

end page

  • 281

volume

  • 1

issue

  • 6