Decoding genetic complexity in glycogen storage diseases: three novel variants in SLC37A4, GAA, and PHKG2 identified in an Iranian cohort

Neuromuscular Disorders 2026

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Authors: Fatemeh Alian, Volker W. Straub, Ana Töpf, Arefeh Seyedarabi, Mahin Hashemipour, Kolsoum InanlooRahatloo, Mansoor Salehi, Noushin Rostampour
DOI: 10.1016/j.nmd.2026.106363
Cited by: 0
References: 33

Fields of Study & Subjects

Glycogen Storage Diseases and Myoclonus Metabolism and Genetic Disorders Lysosomal Storage Disorders Research

Publication details

Journal / source
Neuromuscular Disorders
Volume
61
Pages
106363–106363
Publication date
29 January 2026
Language
EN