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Serveur d'exploration sur les relations entre la France et l'Australie - Analysis (UK)

Index « Auteurs » - entrée « Robert W. Taylor »
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Robert W. Simms < Robert W. Taylor < Robert W. Williams  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 3.
Ident.Authors (with country if any)Title
000902 (2016) Metodi D. Metodiev [France] ; Kyle Thompson [Royaume-Uni] ; Charlotte L. Alston [Royaume-Uni] ; Andrew A. M. Morris [Royaume-Uni] ; Langping He [Royaume-Uni] ; Zarah Assouline [France] ; Marlène Rio [France] ; Nadia Bahi-Buisson [France] ; Angela Pyle [Royaume-Uni] ; Helen Griffin [Royaume-Uni] ; Stefan Siira [Australie] ; Aleksandra Filipovska [Australie] ; Arnold Munnich [France] ; Patrick F. Chinnery [Royaume-Uni] ; Robert Mcfarland [Royaume-Uni] ; Agnès Rötig [France] ; Robert W. Taylor [Royaume-Uni]Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies
001D92 (2012) Joanna L. Elson [Royaume-Uni] ; Mary G. Sweeney [Royaume-Uni] ; Vincent Procaccio [France] ; John W. Yarham [Royaume-Uni] ; Antonio Salas [Espagne] ; Qing-Peng Kong [République populaire de Chine] ; Francois H. Van Der Westhuizen [Afrique du Sud] ; Robert D. S. Pitceathly [Royaume-Uni] ; David R. Thorburn [Australie] ; Marie T. Lott [États-Unis] ; Douglas C. Wallace [États-Unis] ; Robert W. Taylor [Royaume-Uni] ; Robert Mcfarland [Royaume-Uni]Toward a mtDNA locus‐specific mutation database using the LOVD platform
003379 (2004) Patrick F. Chinnery [Royaume-Uni] ; Salvatore Dimauro [États-Unis] ; Sara Shanske [États-Unis] ; Eric A. Schon [États-Unis] ; Massimo Zeviani [Italie] ; Caterina Mariotti [Italie] ; Fanco Carrara [Italie] ; Anne Lombes [France] ; Pascal Laforet [France] ; Helène Ogier [France] ; Michaela Jaksch [Allemagne] ; Hanns Lochmüller [Allemagne] ; Rita Horvath [Allemagne] ; Marcus Deschauer [Allemagne] ; David R. Thorburn [Australie] ; Lavrence A. Bindoff [Norvège] ; Joanna Poulton [Royaume-Uni] ; Robert W. Taylor [Royaume-Uni] ; John N. S. Matthews [Royaume-Uni] ; Douglass M. Turnbull [Royaume-Uni]Risk of developing a mitochondrial DNA deletion disorder

List of associated KwdEn.i

Nombre de
documents		Descripteur
1Amino Acid Sequence
1Association study
1Bandelt
1Biochem biophys
1Biochemical defect
1Cambridge reference sequence
1Central parkway
1Chinnery
1Clinical diagnosis
1Clinical manifestations
1Common disease
1Complete sequences
1Complex disease
1Current databases
1Database
1Deletion
1Disease progression
1Electron Transport (genetics)
1Elson
1European mtdnas
1External ophthalmoplegia
1Female
1Gene variant databases
1Genes, Recessive (genetics)
1Genet
1Genet elson
1Genet epub
1Genet mcfarland
1Genetic medicine
1Genome
1Genotype
1Haplogroup
1Hgvs guidelines
1Howell
1Human disease
1Human health
1Human mitochondrial
1Human mitochondrial genome database
1Human mtdna
1Human mutation
1Human variome project
1Humans
1Hypertrophic cardiomyopathy
1Infant, Newborn
1Initiation codon
1Lovd
1Lovd database
1Lovd platform
1Male
1Many sequences
1Many years
1Mcfarland
1Medical research council
1Medicine
1Methyltransferases (genetics)
1Mitochondria (metabolism)
1Mitochondrial
1Mitochondrial DNA
1Mitochondrial Diseases (etiology)
1Mitochondrial Diseases (pathology)
1Mitochondrial disease
1Mitochondrial disorder
1Mitochondrial disorders
1Mitochondrial genome
1Mitochondrial research group
1Mitochondrial trna mutations
1Mitomap
1Modular design
1Mtdna
1Mtdna changes
1Mtdna disease
1Mtdna haplogroup
1Mtdna mutations
1Mtdna polymorphisms
1Mtdna region
1Mtdna variants
1Mtdna variation
1Multiple copies
1Mutat
1Mutation
1Mutation (genetics)
1National hospital
1Newcastle university
1Next generation
1Next generation sequencing
1Nucleic acids
1Optic neuropathy
1Pathogenic
1Pathogenic mtdna mutations
1Pathogenic mutation
1Pathogenic mutations
1Pathogenic variant
1Pathogenicity
1Pedigree
1Phenotype
1Phylogeographic analysis
1Polymorphism
1Population variants
1Primary mutation
1Protein Biosynthesis (physiology)

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