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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

Research output: Contribution to journalComment/debate

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

Bibliographical note

Publisher Copyright:
© 2016 The Authors

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Endocrinology

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