A newly identified c.1824_1828dupATACG mutation in exon 13 of the GAA gene in infantile-onset glycogen storage disease type II (Pompe disease)
Crossref DOI link: https://doi.org/10.1007/s11033-014-3500-3
Published Online: 2014-06-30
Published Print: 2014-09
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Aryani, Omid
Manshadi, Masoumeh Dehghan
Tondar, Mahdi
Khalili, Elham
Kamalidehghan, Behnam
Ahmadipour, Fatemeh
Fani, Somayeh
Houshmand, Massoud
Text and Data Mining valid from 2014-06-30