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Q33334349-E1F473BB-39DF-426E-A93F-315B693273C4
Q33334349-E1F473BB-39DF-426E-A93F-315B693273C4
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http://www.wikidata.org/entity/statement/Q33334349-E1F473BB-39DF-426E-A93F-315B693273C4
High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.
P2860
Q33334349-E1F473BB-39DF-426E-A93F-315B693273C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33334349-E1F473BB-39DF-426E-A93F-315B693273C4
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wasDerivedFrom
d1abeb6c07d57f6e1ff49ce132b4c2b61c9d9c22
P2860
Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia: identification, functional characterization, and structural analysis