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.
Erratum to: Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype
A. Bowron,J. Honeychurch,Maggie Williams,Beverley Tsai-Goodman,N. Clayton,Lucy Jones,G. Shortland,S. Qureshi,S. Heales,C. Steward
Published 2015 in Journal of Inherited Metabolic Disease
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PUBLICATION RECORD
- Publication year
2015
- Venue
Journal of Inherited Metabolic Disease
- Publication date
2015-09-15
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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