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A case of patient affected by hirsutism carrying the P482S CYP21 gene mutation associated with loss of heterozygosity (LOH)

✍ Scribed by Paola Concolino; Cinzia Carrozza; Angelo Minucci; Concetta Santonocito; Franco Ameglio; Cecilia Zuppi; Ettore Capoluongo


Book ID
116347132
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
66 KB
Volume
370
Category
Article
ISSN
0009-8981

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