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

J Inherit Metab Dis. 2016 Jan;39(1):151. doi: 10.1007/s10545-015-9891-z.

Ann Bowron^{1

2

3}, Julie Honeychurch⁴, Maggie Williams⁴, Beverley Tsai-Goodman^{5

6}, Nicol Clayton⁵, Lucy Jones⁵, Graham J Shortland⁷, Shakeel A Qureshi⁸, Simon J R Heales^{9

10}, Colin G Steward^{5

11}

¹ Department of Clinical Biochemistry, University Hospitals Bristol NHS Trust, Bristol, BS2 8HW, UK. ann.bowron@bristol.ac.uk.
² NHS Barth Syndrome Service, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Trust, Bristol, BS2 8BJ, UK. ann.bowron@bristol.ac.uk.
³ School of Cellular & Molecular Medicine, School of Medical Sciences, University Walk, Bristol, BS8 1TD, UK. ann.bowron@bristol.ac.uk.
⁴ Bristol Genetics Laboratory, North Bristol NHS Trust, Bristol, BS10 5NB, UK.
⁵ NHS Barth Syndrome Service, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Trust, Bristol, BS2 8BJ, UK.
⁶ Department of Paediatric Cardiology, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Trust, Bristol, BS2 8BJ, UK.
⁷ Department of Metabolic Disease, University Hospitals Wales, Cardiff, CF14 4XW, UK.
⁸ Department of Paediatric Cardiology, Evelina Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, SE1 7EH, UK.
⁹ Department of Chemical Pathology, Great Ormond Street Hospital NHS Foundation Trust, London, WC1N 3JH, UK.
¹⁰ University College London Institute of Child Health, London, WC1N 1EH, UK.
¹¹ School of Cellular & Molecular Medicine, School of Medical Sciences, University Walk, Bristol, BS8 1TD, UK.

No abstract available

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