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1
المصدر: Neuroscience Letters. 566:32-35
مصطلحات موضوعية: Adult, Male, China, Adolescent, Population, Mutation, Missense, Biology, medicine.disease_cause, Young Adult, Exon, Asian People, medicine, Humans, Missense mutation, Myopathy, Central Core, education, Genetics, RYR1, Mutation, education.field_of_study, Genetic heterogeneity, General Neuroscience, Ryanodine Receptor Calcium Release Channel, Exons, equipment and supplies, musculoskeletal system, medicine.disease, Congenital myopathy, Child, Preschool, Multigene Family, Female, Central core disease
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e295b1da7c44a1afdc28e69f9f4dbe94Test
https://doi.org/10.1016/j.neulet.2014.02.015Test -
2
المؤلفون: Norberg, Anna, Forsgren, Lars, Holmberg, Dan, Holmberg, Monica
المصدر: Neuroscience Letters. 396(2):137-142
مصطلحات موضوعية: Blood Proteins/*genetics, Calcium-Binding Proteins/*genetics, Chromosome Aberrations, Chromosomes, Human, Pair 6/*genetics, DNA Mutational Analysis, Female, Gene Deletion, Genetic Predisposition to Disease/epidemiology/*genetics, Heterozygote, Humans, Incidence, Male, Membrane Glycoproteins/*genetics, Metalloendopeptidases/*genetics, Migraine Disorders/epidemiology/*genetics, Multigene Family/genetics, Pedigree, Polymorphism, Single Nucleotide/genetics, Sweden/epidemiology
وصف الملف: print
الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-15297Test
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16378686&dopt=CitationTest -
3
المؤلفون: Anna Norberg, Monica Holmberg, Lars Forsgren, Dan Holmberg
المصدر: Neuroscience Letters. 396:137-142
مصطلحات موضوعية: Male, Heterozygote, Candidate gene, Migraine Disorders, DNA Mutational Analysis, Biology, Polymorphism, Single Nucleotide, Genetic predisposition, medicine, Humans, SNP, Genetic Predisposition to Disease, Genetic association, Chromosome Aberrations, Sweden, Genetics, Membrane Glycoproteins, Incidence, General Neuroscience, Calcium-Binding Proteins, Haplotype, Metalloendopeptidases, Blood Proteins, medicine.disease, Pedigree, Multigene Family, RHAG, biology.protein, Chromosomes, Human, Pair 6, Female, Human genome, Juvenile myoclonic epilepsy, Gene Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32bc25baba2c97590f75c2a5fe73a1f5Test
https://doi.org/10.1016/j.neulet.2005.11.039Test