Items where Author is "InanlooRahatloo, K."
![]() | Up a level |
Group by: Item Type | No Grouping
Number of items: 1.
(2026) Decoding genetic complexity in glycogen storage diseases: three novel variants in SLC37A4, GAA, and PHKG2 identified in an Iranian cohort. Neuromuscular Disorders. p. 8. ISSN 0960-8966


