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Q37022929-38F3DD36-D2E0-4C78-9F6E-A3AAB57FF8C7
Q37022929-38F3DD36-D2E0-4C78-9F6E-A3AAB57FF8C7
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Statement
http://www.wikidata.org/entity/statement/Q37022929-38F3DD36-D2E0-4C78-9F6E-A3AAB57FF8C7
Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes
P2860
Q37022929-38F3DD36-D2E0-4C78-9F6E-A3AAB57FF8C7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37022929-38F3DD36-D2E0-4C78-9F6E-A3AAB57FF8C7
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type
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wasDerivedFrom
1e7e40c70b6bb792e22b82146f050b70bbdffe0c
P2860
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood