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2000 | 1 |
2008 | 1 |
2024 | 0 |
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Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1.
J Clin Invest. 2000 Oct;106(7):897-906. doi: 10.1172/JCI9804.
J Clin Invest. 2000.
PMID: 11018078
Free PMC article.
Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.
Pinney SE, MacMullen C, Becker S, Lin YW, Hanna C, Thornton P, Ganguly A, Shyng SL, Stanley CA.
Pinney SE, et al.
J Clin Invest. 2008 Aug;118(8):2877-86. doi: 10.1172/JCI35414.
J Clin Invest. 2008.
PMID: 18596924
Free PMC article.
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