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A Mutation (Pro-30 to Leu) in CYP 21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele

✍ Scribed by Tusie-Luna, Maria-Teresa; Speiser, Phyllis W.; Dumic, Miro; New, Maria I.; White, Perrin C.

No coin nor oath required. For personal study only.

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