The combination of a propensity for venous thrombosis and seizures has been reported in two unrelated kindreds. Transmission is autosomal recessive. It results from a point mutation of PIGM, which reduces transcription of PIGM and blocks mannosylatio

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syndrome d'hypercoagulabilité par déficit héréditaire en glycosyl phosphatidyl inositol

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point mutation

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mutation ponctuelle

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point mutation

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mutation ponctuelle

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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

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syndrome héréditaire de prédisposition au cancer de l'ovaire

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mutated prion protein gene | mutated PrP gene

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géne de protéine du prion muté

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mutation | gene mutation | genetic mutation

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mutation | mutation génétique

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IN-CONTEXT TRANSLATIONS

Positive selection methodology is also in place to detect point mutations arising in the cII gene of the λ bacteriophage shuttle vector [Big Blue® mouse or rat, and Muta™Mouse (17)] and deletion mutations in the λ red and gam genes [Spi– selection in gpt delta mouse and rat (21) (22) (28)].

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Les méthodes de sélection positive permettent également de détecter les mutations ponctuelles du gène cII du bactériophage λ utilisé comme vecteur navette [souris ou rat Big Blue®, Muta™Mouse (17)] et les délétions sur les gènes λ red et gam [sélection Spi– chez souris et rat gpt delta) (21) (22) (28)].

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Others have searched : point mutation single site mutation base pair substitution gene mutation gene point mutation genetic mutation mutated prp gene mutated prion protein gene mutation substitution mutation Gene point mutation

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Date index: 2021-05-11