Molecular Characterization of TNXA/TNXB Chimeras in CYP21A2 Gene Deletions: High Frequency of Undiagnosed Ehlers-Danlos Syndrome in Congenital Adrenal Hyperplasia Patients
HORMONE RESEARCH IN PAEDIATRICS（2018）
关键词
cyp21a2 gene deletions,congenital adrenal hyperplasia patients,tnxa/tnxb chimeras,ehlers-danlos
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