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A Novel Founder Mutation of CYP21A2 in Patients with CAH due to 21-Hydroxylase Deficiency
A Novel Founder Mutation of CYP21A2 in Patients with CAH due to 21-Hydroxylase Deficiency
2014
Ayşenur Ökten
Gülay Karagüzel
Bayram Toraman
Ersan Kalay
Tugba Dincer
Keywords:
Genetics
Founder mutation
in patient
Medicine
21-Hydroxylase
Correction
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