Vertaling van "mutated prp gene " (Engels → Frans) :

mutated prion protein gene | mutated PrP gene
géne de protéine du prion muté

prion protein gene | PrP gene
gène protéine du prion | gène PrP

PrP gene
gène PRNP | gène de la PrP | gène codant pour la protéine PrP | gène prp

Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec
syndrome héréditaire de prédisposition au cancer de l'ovaire

Describes a rare group of immunodeficiencies due to specific mutations in the inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. The clinical manifestation is my
prédisposition mendélienne liée à l'X aux infections mycobactériennes

mutation | gene mutation | genetic mutation
mutation | mutation génétique

base pair substitution | gene point mutation | point mutation | substitution mutation
mutation génique ponctuelle | mutation ponctuelle

mutator | mutator gene
gène mutateur | mutateur

A rare familial skeletal dysplasia with characteristics of multiple epiphyseal dysplasia with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. A mutation in PTHR1 gene is responsible for this synd
syndrome d'Eiken