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))

Danika Nadeen Senanayake, Eresha A. Jasinge, Kirit Pindolia, Jithangi Wanigasinghe, Kristin Monaghan*, Sharon F. Suchy, Sainan Wei, Subashini Jaysena, Barry Wolf

*Corresponding author for this work

Research output: Contribution to journalComment/debatepeer-review

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 languageEnglish (US)
Pages (from-to)95
Number of pages1
JournalMolecular Genetics and Metabolism Reports
Volume11
DOIs
StatePublished - Jun 2017

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Endocrinology

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