Intractable & Rare Diseases Research
Correction
Correction: Novel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome
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Volume 6 (2017) Issue 3 Pages E1

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Abstract

This corrects the article "Novel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome" in volume 5 on page 214-215.

Keiko Shimojima, Koichi Maruyama, Masahiro Kikuchi, Ayako Imai, Ken Inoue, and Toshiyuki Yamamoto (2016). Novel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome. Intractable Rare Dis Res. 5:214-217.

On page 214, abstract line 10, p.(Gly221Ser) should be p.(Gly147Arg). On page 215, 2.2. Genetic examination lines 12-13, c.661G>A [p.(Gly221Ser)] should be c.439G>A [p.(Gly147Arg)].

© 2017 International Research and Cooperation Association for Bio & Socio-Sciences Advancement
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