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Novel human pathological mutations. Gene Symbol: CYP21A2. Disease: Non-classic 21-hydroxylase deficiency

Authors :
Paola Concolino
Santonocito C
Minucci A
Carrozza C
Zuppi C
Capoluongo E
Giardina B
Source :
Scopus-Elsevier, Europe PubMed Central

Details

Database :
OpenAIRE
Journal :
Scopus-Elsevier, Europe PubMed Central
Accession number :
edsair.dedup.wf.001..90042fc5e198f47662c35ac533cf2225