Abstract
The authors regret that we stated that Patient 2 has the mutation c.1316T > C, p.A439D; however, the patient actually has the mutation c.1316C > A; p.A439D. The authors would like to apologise for any inconvenience caused.
| Original language | English |
|---|---|
| Pages (from-to) | 95 |
| Number of pages | 1 |
| Journal | Molecular Genetics and Metabolism Reports |
| Volume | 11 |
| DOIs |
|
| State | Published - Jun 2017 |
Bibliographical note
Publisher Copyright:© 2016 The Authors
ASJC Scopus subject areas
- Molecular Biology
- Genetics
- Endocrinology
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Dive into the research topics of 'Corrigendum to “First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children” [Mol. Genet. Metab. Rep. 2 (2016) 81–84]((S2214426915000075)(10.1016/j.ymgmr.2015.01.005))'. Together they form a unique fingerprint.Cite this
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