Top

Published in:

Open Access 01-12-2018 | Correction

Correction to: Spectrum of PAH gene variants among a population of Han Chinese patients with phenylketonuria from northern China

Authors: Ning Liu, Qiuying Huang, Qingge Li, Dehua Zhao, Xiaole Li, Lixia Cui, Ying Bai, Yin Feng, Xiangdong Kong

Published in: BMC Medical Genetics | Issue 1/2018

Excerpt

Following publication of the original article [1], the authors reported an error in Table 3 on page 4. Variant No. 18 should be “p.Ser339Phe c.1016C>T” (as given in Number 117 of Additional file 2). Other errors were found in the original Additional file 2, which has been replaced with an updated version (see below). …

Liu N, Huang Q, Li Q, Zhao D, Li X, Cui L, Bai Y, Feng Y, Kong X. Spectrum of PAH gene variants among a population of Han Chinese patients with phenylketonuria from northern China. BMC Med Genet. 2017;18:108. doi: 10.1186/s12881-017-0467-7.

Title: Correction to: Spectrum of PAH gene variants among a population of Han Chinese patients with phenylketonuria from northern China
Authors: Ning Liu
Qiuying Huang
Qingge Li
Dehua Zhao
Xiaole Li
Lixia Cui
Ying Bai
Yin Feng
Xiangdong Kong
Publication date: 01-12-2018
Publisher: BioMed Central
Published in: BMC Medical Genetics / Issue 1/2018
Electronic ISSN: 1471-2350
DOI: https://doi.org/10.1186/s12881-017-0516-2

At a glance: The ONWARDS insulin icodec trials

Springer Medicine

Correction to: Spectrum of PAH gene variants among a population of Han Chinese patients with phenylketonuria from northern China

Excerpt

At a glance: The ONWARDS insulin icodec trials

Springer Medicine

Excerpt

Please log in to get access to this content

Other articles of this Issue 1/2018

Identification of deletion-duplication in HEXA gene in five children with Tay-Sachs disease from India

An unusually high frequency of SCAD deficiency caused by two pathogenic variants in the ACADS gene and its relationship to the ethnic structure in Slovakia

Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report

Genetic analysis and clinical assessment of four patients with Glycogen Storage Disease Type IIIa in China

Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population

Association between acromegaly and a single nucleotide polymorphism (rs2854744) in the IGFBP3 gene