%D8%B7%D9%81%D8%B1%D8%A9_%D9%86%D9%82%D8%B7%D9%8A%D8%A9Ta%C4%8Dkasta_mutacija%D9%BE%D9%86%D8%AA%DB%95_%D8%A8%D8%A7%D8%B2%D8%AF%D8%A7%D9%86Category:Point_mutationPunktmutationPunktmutationPoint_mutationMutaci%C3%B3n_gen%C3%A9tica%D8%AC%D9%87%D8%B4_%D9%86%D9%82%D8%B7%D9%87%E2%80%8C%D8%A7%DB%8CPistemutaatioMutation_ponctuelleMutaci%C3%B3n_puntual%E7%82%B9%E7%AA%81%E7%84%B6%E5%A4%89%E7%95%B0%EC%A0%90_%EB%8F%8C%EC%97%B0%EB%B3%80%EC%9D%B4PuntmutatieMutacja_punktowaMuta%C3%A7%C3%A3o_pontual%D0%A2%D0%BE%D1%87%D0%B5%D1%87%D0%BD%D0%B0%D1%8F_%D0%BC%D1%83%D1%82%D0%B0%D1%86%D0%B8%D1%8FTa%C4%8Dkasta_mutacijaPoint_mutation%D0%93%D0%B5%D0%BD%D1%81%D0%BA%D0%B5_%D0%BC%D1%83%D1%82%D0%B0%D1%86%D0%B8%D1%98%D0%B5PunktmutationNokta_mutasyon%D8%B7%D9%81%D8%B1%DB%81_%D9%86%D9%82%D8%B7%DB%8C%DB%81%C4%90%E1%BB%99t_bi%E1%BA%BFn_%C4%91i%E1%BB%83mQ1415380%E9%BB%9E%E7%AA%81%E8%AE%8A
about
P828
Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated populationDigital PCRType I transglutaminase accumulation in the endoplasmic reticulum may be an underlying cause of autosomal recessive congenital ichthyosis.Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disordersDevelopment of a Novel Loop-Mediated Isothermal Amplification Method to Detect Guiana Extended-Spectrum (GES) β-Lactamase Genes inPoint mutation detection by economic HRM protocol primer designProgrammable Base Editing of the Sheep Genome Revealed No Genome-Wide Off-Target MutationsWithin-population variability in a moth sex pheromone blend, part 2: selection towards fixationShort-Homology-Mediated CRISPR/Cas9-Based Method for Genome Editing in Fission YeastMolecular simulation investigation on the interaction between barrier-to-autointegration factor dimer or its Gly25Glu mutant and LEM domain of emerin
P921
Q24678416-33f90f18-4530-4411-0a0a-e183920771b3Q24685020-e9f7f137-4b81-0fd1-7b2b-f24f5a31f629Q34181509-fa6bd26d-4443-1f05-3fc6-d51d55aae815Q57812209-1262C68A-5250-48CA-8EC3-6289FE2B05FEQ61800051-8F91EE5E-2633-427B-9009-F9FD341C0CB7Q64062253-D7F70D59-900B-4E2D-BBAB-BA1B6573AC75Q64086708-13EE9C06-5B92-4046-850D-203D28744D55Q64100058-64CB8623-1983-4F1B-A290-80612EAF7517Q64230645-91C45B5A-A8C9-4F92-9EF2-6E897DE1B841Q64390210-F24B7A78-A2C1-4E79-8085-8A47B2DBB9BE
P921
description
Störung einer Genreplikaton
@de
changement de la structure du ...... nucléotides (entre un et dix)
@fr
mutasjon i einskildgen
@nn
mutation of a single gene
@en
name
Genska mutacija
@bs
Genske mutacije
@sh
Genske mutacije
@sr-el
Mutación genética
@es
Mutación puntual
@gl
Mutacja punktowa
@pl
Mutação pontual
@pt
Nokta mutasyon
@tr
Pistemutaatio
@fi
Punktmutation
@da
type
label
Genska mutacija
@bs
Genske mutacije
@sh
Genske mutacije
@sr-el
Mutación genética
@es
Mutación puntual
@gl
Mutacja punktowa
@pl
Mutação pontual
@pt
Nokta mutasyon
@tr
Pistemutaatio
@fi
Punktmutation
@da
altLabel
Mutacion genetica
@es
Nokta mutasyonlar
@tr
Nokta mutasyonu
@tr
Noktasal mutasyon
@tr
Tačkasta mutacija
@bs
Tačkasta mutacija
@sh
mutations ponctuelles
@fr
point mutations
@en
Мутация замены оснований
@ru
Точковая мутация
@ru
prefLabel
Genska mutacija
@bs
Genske mutacije
@sh
Genske mutacije
@sr-el
Mutación genética
@es
Mutación puntual
@gl
Mutacja punktowa
@pl
Mutação pontual
@pt
Nokta mutasyon
@tr
Pistemutaatio
@fi
Punktmutation
@da
P486
P6366
P646
P672
P1417
science/point-mutation
P373
Point mutation
P3827
point-mutation
P486
P5082
punktmutasjon
P6366
P646
P672
G05.365.590.675