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Predominance of the c.648G > T G6PC gene mutation and late complications in Korean patients with glycogen storage disease type Ia.

Orphanet J Rare Dis · 2020 · PMC7014716 · PMID 32046761

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This might be due to the more delayed diagnosis in males (16.4 ± 10.9 years) compared to females (15.0 ± 13.1 years), although this did not reach statistical significance.

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