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pyridoxal phosphate"
Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolism |
Keller Natalie1, Mendoza-Ferreira Natalia1, Maroofian Reza2, Chelban Viorica34, Khalil Youssef5, Mills Philippa B.5, Boostani Reza6, Torbati Paria Najarzadeh7, Karimiani Ehsan Ghayoor2, Thiele Holger1, Houlden Henry H.8, Wirth Brunhilde1, Karakaya Mert1 |
1 University of Cologne, 2 St. George's University of London, 3 UCL Queen Square Institute of Neurology, 4 Emergency Institute of Medicine, 6 Mashhad University of Medical Sciences, 7 Next Generation Genetic Polyclinic, Mashhad,
|
Neuromuscular Disorders |
Nr. 7(30) / 2020 / ISSN 0960-8966 /ISSNe 1874-2364 |
Disponibil online 9 October, 2020. Descarcări-0. Vizualizări-414 |
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