Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolism-Reference-Cited by-同舟云学术

Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolism

Published:2020-07 Issue:7 Volume:30 Page:583-589
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Keller Natalie,Mendoza-Ferreira Natalia,Maroofian Reza,Chelban Viorica,Khalil Youssef,Mills Philippa B.,Boostani Reza,Torbati Paria Najarzadeh,Karimiani Ehsan Ghayoor,Thiele Holger,Houlden Henry,Wirth Brunhilde,Karakaya Mert

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference17 articles.

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4. Pyridoxal phosphokinases. II. Effects of inhibitors;McCormick;J Biol Chem,1961

5. Genomic organization, tissue distribution and deletion mutation of human pyridoxine 5′-phosphate oxidase;Kang;Eur J Biochem,2004

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