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The Journal of Clinical Pharmacology, ISSN 0091-2700, 10/2018, Volume 58, Issue 10, pp. 1361 - 1370
Journal Article
Journal Article
Helicobacter, ISSN 1083-4389, 10/2017, Volume 22, Issue 5, pp. e12415 - n/a
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 04/2018, Volume 63, Issue 4, pp. 417 - 423
Autosomal recessive cerebellar ataxias (ARCAs) are clinically and genetically heterogeneous neurological disorders. Through whole-exome sequencing of Japanese... 
XERODERMA-PIGMENTOSUM | VARIANTS | DISEASE | GENETICS & HEREDITY | DNA-REPAIR ENDONUCLEASE | COMPLEMENTATION GROUP-F | FANCONI-ANEMIA | XPF | Ataxia | Mutation
Journal Article
PLoS genetics, ISSN 1553-7404, 04/2017, Volume 13, Issue 4, p. e1006730
[This corrects the article DOI: 10.1371/journal.pgen.1006546.]. 
Journal Article
Muscle & Nerve, ISSN 0148-639X, 09/2016, Volume 54, Issue 3, pp. 398 - 404
Journal Article
Journal Article
Nature Communications, ISSN 2041-1723, 12/2019, Volume 10, Issue 1, pp. 2506 - 14
Journal Article
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 06/2019, Volume 14, Issue 1, pp. 155 - 9
BackgroundSporadic inclusion body myositis (sIBM) is the most prevalent muscle disease in elderly people, affecting the daily activities. sIBM is progressive... 
DYSPHAGIA | MEDICINE, RESEARCH & EXPERIMENTAL | Multicenter survey | Questionnaire | Sporadic inclusion body myositis | Muscle diseasef | INTRAVENOUS IMMUNOGLOBULIN | GENETICS & HEREDITY | Aging | MUSCLE | HEPATITIS-C | Myositis | Care and treatment | Research
Journal Article
Journal Article
Muscle & Nerve, ISSN 0148-639X, 09/2016, Volume 54, Issue 3, pp. 398 - 404
Journal Article