Resumen
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.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 95 |
| Número de páginas | 1 |
| Publicación | Molecular Genetics and Metabolism Reports |
| Volumen | 11 |
| DOI |
|
| Estado | Published - jun 2017 |
Nota bibliográfica
Publisher Copyright:© 2016 The Authors
ASJC Scopus subject areas
- Molecular Biology
- Genetics
- Endocrinology
Huella
Profundice en los temas de investigación de '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))'. En conjunto forman una huella única.Citar esto
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