(2026). Familial isolated 17,20-lyase deficiency in three siblings caused by a CYP17A1 mutation. Endocrinology, Diabetes & Metabolism Case Reports.
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Chicago Style (17th ed.) Citation
"Familial Isolated 17,20-lyase Deficiency in Three Siblings Caused by a CYP17A1 Mutation."
Endocrinology, Diabetes & Metabolism Case Reports 2026.
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MLA (9th ed.) Citation
"Familial Isolated 17,20-lyase Deficiency in Three Siblings Caused by a CYP17A1 Mutation."
Endocrinology, Diabetes & Metabolism Case Reports, 2026.
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Warning: These citations may not always be 100% accurate.