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Published Erratum
. 2016 Aug 4;2(4):e86.
doi: 10.1212/NXG.0000000000000086. eCollection 2016 Aug.

Erratum: Mutation of TBCK causes a rare recessive developmental disorder

No authors listed
Published Erratum

Erratum: Mutation of TBCK causes a rare recessive developmental disorder

No authors listed. Neurol Genet. .

Abstract

[This corrects the article on p. e76 in vol. 2, PMID: 27275012.].

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Figures

Figure.
Figure.. Pedigree of the family studied, photographs, and identification of a homozygous mutation in TBCK
(A) Pedigree showing complete segregation of the TBCK c.614_617del; p.205_206del mutation in the family members available for analysis. (B) Photographs of the affected siblings. (C) Sanger sequencing traces for all family members available for analysis (2 affected siblings, the parents, and 1 unaffected sibling). The 3 upper chromatograms represent a reference sequence and the unaffected family members where the heterozygous deletion can be observed. The 2 lower chromatograms represent 2 of the affected siblings where the same deletion can be observed in homozygosity.
See this image and copyright information in PMC

Erratum for

References

    1. Guerreiro RJ, Brown R, Dian D, de Goede C, Bras J, Mole SE. Mutation of TBCK causes a rare recessive developmental disorder. Neurol Genet 2016;2:e76. doi: 10.1212/NXG.0000000000000076. - DOI - PMC - PubMed

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