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.
. 2016 Apr 12;11:95. doi: 10.1016/j.ymgmr.2016.04.001
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]
Danika Nadeen Senanayake
a, Eresha A Jasinge
b, Kirit Pindolia
c,d, Jithangi Wanigasinghe
e, Kristin Monaghan
f,⁎, Sharon F Suchy
f, Sainan Wei
g, Subashini Jaysena
b, Barry Wolf
c,d
Danika Nadeen Senanayake
aDepartment of Chemical Pathology, North Columbo Teaching Hospital, Columbo, Sri Lanka
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Eresha A Jasinge
bChemical Pathology, Lady Ridgeway Hospital for Children, Colombo, Sri Lanka
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Kirit Pindolia
cDepartment of Research Administration, Henry Ford Health System, Detroit, MI 48202, United States
dCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, United States
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Jithangi Wanigasinghe
ePediatric Neurology, University of Colombo, Columbo, Sri Lanka
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Sainan Wei
gDepartment of Pediatrics and Human Development, Michigan State University, East Lansing, MI 48824, United States
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Subashini Jaysena
bChemical Pathology, Lady Ridgeway Hospital for Children, Colombo, Sri Lanka
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Barry Wolf
cDepartment of Research Administration, Henry Ford Health System, Detroit, MI 48202, United States
dCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, United States
Find articles by Barry Wolf
aDepartment of Chemical Pathology, North Columbo Teaching Hospital, Columbo, Sri Lanka
bChemical Pathology, Lady Ridgeway Hospital for Children, Colombo, Sri Lanka
cDepartment of Research Administration, Henry Ford Health System, Detroit, MI 48202, United States
dCenter for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, United States
ePediatric Neurology, University of Colombo, Columbo, Sri Lanka
fGeneDx, Gaithersburg, MD 20877, United States
gDepartment of Pediatrics and Human Development, Michigan State University, East Lansing, MI 48824, United States
⁎
Corresponding author at: GeneDx, Gaithersburg, MD, United States.GeneDxGaithersburgMDUnited States
Collection date 2017 Jun.
© 2016 The Authors
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
PMCID: PMC5470936 PMID: 28653700
This corrects the article "First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children" in volume 2 on page 81.