Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran
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H. Galehdari | M. Zamani | A. Sedaghat | T. Seifi | S. Sedighzadeh | Samira Negahdari | Jawaher Zeighami | A. Saberi | M. Hamid | G. Shariati | A. Papi
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