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GNAS Mutations in Fibrous Dysplasia: A Comparative Study of Standard Sequencing and Locked Nucleic Acid PCR Sequencing on Decalcified and Non-Decalcified Formalin Fixed Paraffin Embedded Tissues

It is well-known that fibrous dysplasia is characterized by the presence of activating mutations involving G-nucleotide binding protein alpha sub unit (GNAS) involving codon R201 and rarely codon 227 with a mutation frequency between 45–93%. Herein, we investigate the sensitivity of detection of GNA...

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Publicado en:Appl Immunohistochem Mol Morphol
Autores principales: Jour, George, Oultache, Alifya, Sadowska, Justyna, Mitchell, Talia, Healey, John, Nafa, Khedoudja, Hameed, Meera
Formato: Artigo
Lenguaje:Inglês
Publicado: 2016
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5563825/
https://ncbi.nlm.nih.gov/pubmed/26574629
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PAI.0000000000000242
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