Author

Emna Hamdeni

Institutions: Tunis University, Faculté de médecine de Tunis, Tunis El Manar University

Observed institutions: Tunis University, Faculté de médecine de Tunis, Tunis El Manar University

OpenAlex ID: A5092662622

Constitutional mismatch repair deficiency syndrome with atypical features caused by a homozygous MLH1 missense variant (c.1918C>A, p.(Pro640Thr)): a case report

2023 · Firas Akrout, Ahlem Achour, et al. · Frontiers in Oncology · 2

Works count: 1

Citation count: 2

H-index: 1

I10-index: