Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype Journal Articles Refereed uri icon

Overview

Authors

  • Authorship

    • ALSTON CL
    • CIARA E
    • CASSIMAN D
    • ROMAIN N
    • YARHAM JW
    • HE L
    • DE PAEPE B
    • VANLANDER AV
    • SENECA S
    • FEICHTINGER RG
    • POSKI R
    • DR Alison Compton
    • ROKICKI D
    • PRONICKA E
    • HALLER RG
    • VAN HOVE JLK
    • PROF Melanie Bahlo
    • MAYR JA
    • VAN COSTER R
    • PROKISCH H
    • WITTIG I
    • RYAN MT
    • FORMOSA LE
    • PROF David Thorburn
    • TAYLOR RW
    • STRECKER V
    • OLAHOVA M
    • HAACK TB
    • SMET J
    • STOUFFS K
    • DIAKUMIS P

Published in

  • American Journal of Human Genetics

Time

Date/time value

  • 2016

Identity

Digital Object Identifier (DOI)

  • 10.1016/j.ajhg.2016.05.021

Additional Document Info

Parent Title

  • AMERICAN JOURNAL OF HUMAN GENETICS

Volume

  • 99

Issue

  • 1

Publisher

  • University of Chicago Press