Mutational spectrum of the phenylalanine hydroxylase gene in patients with phenylketonuria in the central region of China-Reference-Cited by-同舟云学术

Mutational spectrum of the phenylalanine hydroxylase gene in patients with phenylketonuria in the central region of China

Published:2018-02-01 Issue:3 Volume:78 Page:211-218
ISSN:0036-5513
Container-title:Scandinavian Journal of Clinical and Laboratory Investigation
language:en
Short-container-title:Scandinavian Journal of Clinical and Laboratory Investigation

Author:

Zhang Zhan¹²^ORCID,Gao Jun-Jun¹,Feng Yang¹,Zhu Lin-Lin³,Yan Huan¹,Shi Xu-Feng⁴,Chang Ai-Min¹,Shi Ying¹,Wang Ping¹

Affiliation:

1. The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China;

2. Shangqiu Medical College, Shangqiu, China;

3. School of Laboratory Medicine, Xinxiang Medical University, Xinxiang, China;

4. Department of Obstetrics, Henan Province People’s Hospital, Zhengzhou, China

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,General Medicine

Link

Reference37 articles.

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