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Journal of Inherited Metabolic Disease

, Volume 39, Issue 1, pp 151–151 | Cite as

Erratum to: Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype

  • Ann Bowron
  • Julie Honeychurch
  • Maggie Williams
  • Beverley Tsai-Goodman
  • Nicol Clayton
  • Lucy Jones
  • Graham J. Shortland
  • Shakeel A. Qureshi
  • Simon J. R. Heales
  • Colin G. Steward
Erratum
  • 734 Downloads

Erratum to: J Inherit Metab Dis (2015) 38:279–286

DOI 10.1007/s10545-014-9747-y

The original version of this article unfortunately contained a mistake. The reference by Whited is incomplete. The corrected reference is:

Whited K, Baile MG, Currier P, Claypool SM (2013) Seven functional classes of Barth syndrome mutation. Human Molecular Genetics 22:483–492.

Copyright information

© SSIEM 2015

Authors and Affiliations

  • Ann Bowron
    • 1
    • 2
    • 3
  • Julie Honeychurch
    • 4
  • Maggie Williams
    • 4
  • Beverley Tsai-Goodman
    • 2
    • 5
  • Nicol Clayton
    • 2
  • Lucy Jones
    • 2
  • Graham J. Shortland
    • 6
  • Shakeel A. Qureshi
    • 7
  • Simon J. R. Heales
    • 8
    • 9
  • Colin G. Steward
    • 2
    • 3
  1. 1.Department of Clinical BiochemistryUniversity Hospitals Bristol NHS TrustBristolUK
  2. 2.NHS Barth Syndrome Service, Bristol Royal Hospital for ChildrenUniversity Hospitals Bristol NHS TrustBristolUK
  3. 3.School of Cellular & Molecular Medicine, School of Medical SciencesBristolUK
  4. 4.Bristol Genetics LaboratoryNorth Bristol NHS TrustBristolUK
  5. 5.Department of Paediatric Cardiology, Bristol Royal Hospital for ChildrenUniversity Hospitals Bristol NHS TrustBristolUK
  6. 6.Department of Metabolic DiseaseUniversity Hospitals WalesCardiffUK
  7. 7.Department of Paediatric Cardiology, Evelina Children’s HospitalGuy’s and St Thomas’ NHS Foundation TrustLondonUK
  8. 8.Department of Chemical PathologyGreat Ormond Street Hospital NHS Foundation TrustLondonUK
  9. 9.University College London Institute of Child HealthLondonUK

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