-
1دورية أكاديمية
المصدر: Annals of Movement Disorders, Vol 5, Iss 2, Pp 93-105 (2022)
مصطلحات موضوعية: dystonia, ethnicity, parkinsonism, tremor, trinucleotide repeat disorders, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
العلاقة: http://www.aomd.in/article.asp?issn=2590-3446;year=2022;volume=5;issue=2;spage=93;epage=105;aulast=RadhakrishnanTest; https://doaj.org/toc/2590-3446Test; https://doaj.org/toc/2590-3454Test
-
2دورية أكاديمية
المؤلفون: Bhavna S Rao, Arokiasamy Tharigopala, Sudhir R Rachapalli, Rama Rajagopal, Nagasamy Soumittra
المصدر: Indian Journal of Ophthalmology, Vol 65, Iss 10, Pp 931-935 (2017)
مصطلحات موضوعية: Fuchs endothelial corneal dystrophy, SNP, TCF4 gene, trinucleotide repeat, Ophthalmology, RE1-994
وصف الملف: electronic resource
العلاقة: http://www.ijo.in/article.asp?issn=0301-4738;year=2017;volume=65;issue=10;spage=931;epage=935;aulast=RaoTest; https://doaj.org/toc/0301-4738Test; https://doaj.org/toc/1998-3689Test
-
3دورية أكاديمية
المؤلفون: Kalyan B Bhattacharyya
المصدر: Annals of Indian Academy of Neurology, Vol 19, Iss 1, Pp 25-28 (2016)
مصطلحات موضوعية: Huntington, Wexler, Gusella, trinucleotide repeat length, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
العلاقة: http://www.annalsofian.org/article.asp?issn=0972-2327;year=2016;volume=19;issue=1;spage=25;epage=28;aulast=BhattacharyyaTest; https://doaj.org/toc/0972-2327Test; https://doaj.org/toc/1998-3549Test
-
4
المؤلفون: Ajay Garg, Pooja Sharma, Uzma Shamim, Mohammed Faruq, Biswaroop Chakrabarty, Sheffali Gulati, A.K. Srivastava, RajaG Shaikh, AkhileshK Sonakar, Vaishakh Anand, Istaq Ahmad
المصدر: Annals of Movement Disorders, Vol 3, Iss 1, Pp 60-64 (2020)
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Ataxia, Cognitive Neuroscience, dentatorubral–pallidoluysian atrophy, Neuroscience (miscellaneous), Choreoathetosis, lcsh:RC346-429, Atrophy, Intellectual disability, medicine, Dementia, cag repeats, lcsh:Neurology. Diseases of the nervous system, Dentatorubral-pallidoluysian atrophy, business.industry, indian population, medicine.disease, Neurology, trinucleotide repeats, Myoclonic epilepsy, Surgery, Neurology (clinical), medicine.symptom, Trinucleotide repeat expansion, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e77574b92a9540088710d9cc49a50dfTest
http://www.aomd.in/article.asp?issn=2590-3446;year=2020;volume=3;issue=1;spage=60;epage=64;aulast=SharmaTest -
5دورية أكاديمية
المؤلفون: Jin Zhang, Weihong Gu, Ying Hao, Yuanyuan Chen
المصدر: Annals of Indian Academy of Neurology, Vol 16, Iss 4, Pp 703-704 (2013)
مصطلحات موضوعية: Neuroimage, spinocerebellar ataxia 17, TATA-box binding protein gene, trinucleotide repeat, Neurology. Diseases of the nervous system, RC346-429
العلاقة: http://www.annalsofian.org/article.asp?issn=0972-2327;year=2013;volume=16;issue=4;spage=703;epage=704;aulast=ZhangTest; https://doaj.org/toc/0972-2327Test; https://doaj.org/toc/1998-3549Test; https://doaj.org/article/15482eae828f46d0bdfff784a92aa8c2Test
الإتاحة: https://doi.org/10.4103/0972-2327.120457Test
https://doaj.org/article/15482eae828f46d0bdfff784a92aa8c2Test -
6
المؤلفون: Achal Kumar Srivastava, Suman Singh, Tanuj Dada, Madhuri Behari, Ajay Garg, Rohit Gupta, Mitali Mukerji, Mohammed Faruq
المصدر: Indian Journal of Medical Research, Vol 141, Iss 2, Pp 187-198 (2015)
The Indian Journal of Medical Research
Scopus-Elsevierمصطلحات موضوعية: Adult, Male, Indian population, Retinal degeneration, Pediatrics, medicine.medical_specialty, Adolescent, Population, India, CAG repeats, lcsh:Medicine, genotype-phenotype correlation, Biology, General Biochemistry, Genetics and Molecular Biology, CAG repeats - genotype-phenotype correlation - Indian population - SCA7 - spinocerebellar ataxia, spinocerebellar ataxia, Ethnicity, SCA7, medicine, Humans, Spinocerebellar Ataxias, Spasticity, Allele, Child, education, Alleles, Genetic Association Studies, Ataxin-7, Genetics, education.field_of_study, Cerebellar ataxia, lcsh:R, General Medicine, Middle Aged, medicine.disease, Pedigree, Phenotype, Child, Preschool, Mutation, Spinocerebellar ataxia, Female, Original Article, Age of onset, medicine.symptom, Trinucleotide Repeat Expansion, Asymptomatic carrier
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0464c4cb1c8a8e7359d7f3b02fe00dcTest
http://www.ijmr.org.in/article.asp?issn=0971-5916;year=2015;volume=141;issue=2;spage=187;epage=198;aulast=FaruqTest