Persistent URL of this record https://hdl.handle.net/1887/3731509
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- fonc-13-1195814
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Constitutional mismatch repair deficiency syndrome with atypical features caused by a homozygous MLH1 missense variant (c.1918C>A, p.(Pro640Thr)) a case report
- All authors
- Akrout, F.; Achour, A.; Tops, C.M.J.; Gallon, R.; Meddeb, R.; Achoura, S.; Rekaya, M. ben; Hamdeni, E.; Rammeh, S.; Chkili, R.; Mansouri, N.; Belguith, N.; Mrad, R.
- Date
- 2023-08-17
- Journal
- Frontiers in Oncology
- Volume
- 13