Inhibin α-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers

The R337H TP53 mutation is a low-penetrance molecular defect that predisposes to adrenocortical tumour (ACT) formation in Brazilian and possibly other populations. Additional genetic defects may be responsible for the variable expression of ACTs in these cases. The inhibin α-subunit gene (INHA) on 2...

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מידע ביבליוגרפי
Main Authors: Longui, C, Lemos-Marini, S, Figueiredo, B, Mendonca, B, Castro, M, Liberatore, R, Watanabe, C, Lancellotti, C, Rocha, M, Melo, M, Monte, O, Calliari, L, Guerra-Junior, G, Baptista, M, Sbragia-Neto, L, Latronico, A, Moreira, A, Tardelli, A, Nigri, A, Taymans, S, Stratakis, C
פורמט: Artigo
שפה:Inglês
יצא לאור: BMJ Group 2004
נושאים:
Short Report
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735776/
https://ncbi.nlm.nih.gov/pubmed/15121773
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.018978
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