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Erratum to: Barth syndrome without tetralinoleoyl cardiolipin deficiency: a possible ameliorated phenotype
- Source :
- Journal of Inherited Metabolic Disease. 39:151-151
- Publication Year :
- 2015
- Publisher :
- Wiley, 2015.
-
Abstract
- 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.
- Subjects :
- 0301 basic medicine
medicine.medical_specialty
business.industry
Barth syndrome
030105 genetics & heredity
Bioinformatics
medicine.disease
Phenotype
Human genetics
03 medical and health sciences
chemistry.chemical_compound
Endocrinology
chemistry
Internal medicine
Molecular genetics
Genetics
medicine
Cardiolipin
business
Genetics (clinical)
Subjects
Details
- ISSN :
- 15732665 and 01418955
- Volume :
- 39
- Database :
- OpenAIRE
- Journal :
- Journal of Inherited Metabolic Disease
- Accession number :
- edsair.doi...........007a48a9968fd622bed073cf33e511c2
- Full Text :
- https://doi.org/10.1007/s10545-015-9891-z