Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lauria Batamba Bouya"'
Publikováno v:
Global Medical Genetics, Vol 10, Iss 01, Pp 001-005 (2023)
Background Lynch syndrome (LS) is an autosomal dominant condition due to the germline mutation in the mismatch repair (MMR) genes including MLH1, MSH2, MSH6, and PMS2 (post-meiotic segregation increased 2). The MMR mutation carriers have high risk fo
Externí odkaz:
https://doaj.org/article/ff247c6dc8c14d4596d3d1046332de02
Autor:
J. F. Peko, Irène Patricia Lucienne Ondima, Aimé Lumaka Zola, Lauria Batamba Bouya, Henriette Poaty, Deby Gassaye, Arnaud Mongo-Onkouo
Publikováno v:
Gene Reports. 23:101141
Background Juvenile polyposis syndrome (JPS) is a rare genetic disorder due to germline mutations in BMPR1A or in SMAD4 that are both tumor suppressor genes. The main clinical manifestation is the presence of multiple hamartomatous polyps preferentia
Autor:
Poaty, Henriette1,2,3 henriettepoaty@gmail.com, Bouya, Lauria Batamba3, Lumaka, Aimé4,5, Mongo-Onkouo, Arnaud3,6, Gassaye, Deby3,6
Publikováno v:
Global Medical Genetics. Jan2023, Vol. 10 Issue 1, p1-5. 5p.