A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma - Aix-Marseille Université Access content directly
Journal Articles Genes Year : 2022

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma

Maria Kabbage
  • Function : Author
Jihenne Ben Aissa-Haj
  • Function : Author
Houcemeddine Othman
  • Function : Author
Amira Jaballah-Gabteni
  • Function : Author
Sarra Laarayedh
  • Function : Author
Mouna Medhioub
  • Function : Author
Haifa Tounsi Kettiti
  • Function : Author
Amal Khsiba
  • Function : Author
Moufida Mahmoudi
  • Function : Author
Houda Belfekih
  • Function : Author
Afifa Maaloul
  • Function : Author
Hassen Touinsi
  • Function : Author
Lamine Hamzaoui
  • Function : Author
Emna Chelbi
  • Function : Author
Sonia Abdelhak
  • Function : Author
Mohamed Samir Boubaker
  • Function : Author
Mohamed Mousaddak Azzouz
  • Function : Author

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Genetics
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Dates and versions

hal-03780358 , version 1 (24-02-2023)

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Maria Kabbage, Jihenne Ben Aissa-Haj, Houcemeddine Othman, Amira Jaballah-Gabteni, Sarra Laarayedh, et al.. A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrome II Screening in Tunisia: A Case of Diffuse Gastric Carcinoma. Genes, 2022, 13 (8), ⟨10.3390/genes13081355⟩. ⟨hal-03780358⟩

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