<abstract xml:lang="en" xmlns="http://www.w3.org/1999/xhtml"><p>Recessively inherited mutations in the base excision repair gene <italic>MYH</italic> are related to <italic>MYH</italic>-associated polyposis (MAP). We report a Moroccan patient who carried the mutation p.Tyr165Cys. Genetic testing for MYH mutations should have important implications for accurate genetic counseling, and cancer surveillance for patients with colorectal cancers and their family members in Morocco.</p></abstract>

Recessively inherited mutations in the base excision repair gene MYH are related to MYH-associated polyposis (MAP). We report a Moroccan patient who carried the mutation p.Tyr165Cys. Genetic testing for MYH mutations should have important implications for accurate genetic counseling, and cancer surveillance for patients with colorectal cancers and their family members in Morocco.

MYH Associated Polyposis with a p.Tyr165Cys Mutation in a Moroccan Patient

Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco

Laboratoire de Génomique Humaine, Faculté de Médecine et de Pharmacie, Université Mohamed V, Rabat, Morocco

Balkan Journal of Medical Genetics

{"article-title":"MYH Associated Polyposis with a p.Tyr165Cys Mutation in a Moroccan Patient"}

Recessively inherited mutations in the base excision repair gene MYH are related to MYH-associated polyposis (MAP). We report a Moroccan patient who carried...

MYH Associated Polyposis with a p.Tyr165Cys Mutation in a Moroccan Patient

Online veröffentlicht: 19. Feb. 2010

Seitenbereich: 65 - 67

DOI: https://doi.org/10.2478/v10034-010-0010-z

Schlüsselwörter
Colorectal cancer, MYH gene, p.Tyr165 Cys mutation

This content is open access.

MYH Associated Polyposis with a p.Tyr165Cys Mutation in a Moroccan Patient

Online veröffentlicht: 19. Feb. 2010

Seitenbereich: 65 - 67

DOI: https://doi.org/10.2478/v10034-010-0010-z

SchlüsselwörterColorectal cancer, MYH gene, p.Tyr165 Cys mutation

This content is open access.

Schlüsselwörter
Colorectal cancer, MYH gene, p.Tyr165 Cys mutation