Identification of new variants in patients with mucopolysaccharidosis in consanguineous Iranian families by Rezvan Zabihi, Mina Zamani, Mina Zamani, Majid Aminzadeh, Niloofar Chamanrou, Niloofar Chamanrou, Niloofar Chamanrou, Fatemeh Zahra Kiani, Fatemeh Zahra Kiani, Tahere Seifi, Tahere Seifi, Jawaher Zeighami, Tahere Yadegari, Alireza Sedaghat, Alireza Sedaghat, Alihossein Saberi, Alihossein Saberi, Mohammad Hamid, Gholamreza Shariati, Gholamreza Shariati, Hamid Galehdari

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Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran by Atefe Papi, Mina Zamani, Gholamreza Shariati, Alireza Sedaghat, Tahere Seifi, Samira Negahdari, Sahar Sadat Sedighzadeh, Jawaher Zeighami, Alihossein Saberi, Mohammad Hamid, Hamid Galehdari

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