Transient developmental delays in infants with Duarte-2 variant galactosemia-Reference-Cited by-同舟云学术

Transient developmental delays in infants with Duarte-2 variant galactosemia

Published:2021-09 Issue:1-2 Volume:134 Page:132-138
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Waisbren Susan E.,Tran Catherine,Demirbas Didem,Gubbels Cynthia S.,Hsiao Margaret,Daesety Vikram,Berry Gerard T.

Funder

National Center for Advancing Translational Sciences

Harvard University

National Institutes of Health

Harvard Catalyst

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference44 articles.

1. Galactosemia;Walter,2014

2. Disorders of galactose metabolism;Berry,2016

3. Classic galactosemia and clinical variant galactosemia;Berry,2000

4. Developmental outcomes in Duarte galactosemia;Carlock;Pediatrics,2019

5. J.L. Fridovich-Keil, M.J. Gambello, R.H. Singh, J.D. Sharer, Duarte Variant Galactosemia, 1993rd–2021st ed., Seattle (WA): University of Washington, Seattle, n.d. https://www.ncbi.nlm.nih.gov/books/NBK258640/.

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Analysis of Gut Microbiota in <i>Galt</i> Editing Mice;Hans Journal of Medicinal Chemistry;2024

2. Carrier burden of over 300 diseases in Han Chinese identified by expanded carrier testing of 300 couples using assisted reproductive technology;Journal of Assisted Reproduction and Genetics;2023-07-14

3. Endocrine Disorders in a Newborn with Heterozygous Galactosemia, Down Syndrome and Complex Cardiac Malformation: Case Report;Medicina;2023-04-28

4. Incidental molecular diagnoses and heterozygous risk alleles in a carrier screening cohort;Genetics in Medicine;2023-02

5. Galactosemia;Genetic Syndromes;2023