دورية أكاديمية
Application of whole exome sequencing to a rare inherited metabolic disease with neurological and gastrointestinal manifestations: A congenital disorder of glycosylation mimicking glycogen storage disease
| العنوان: | Application of whole exome sequencing to a rare inherited metabolic disease with neurological and gastrointestinal manifestations: A congenital disorder of glycosylation mimicking glycogen storage disease |
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| المؤلفون: | Choi, Rihwa, Woo, Hye In, Choe, Byung-Ho, Park, Seungman, Yoon, Yeomin, Ki, Chang-Seok, Lee, Soo-Youn, Kim, Jong-Won, Song, Junghan, Kim, Dong Sub, Kwon, Soonhak, Park, Hyung-Doo |
| المساهمون: | Ministry of Health and Welfare |
| المصدر: | Clinica Chimica Acta ; volume 444, page 50-53 ; ISSN 0009-8981 |
| بيانات النشر: | Elsevier BV |
| سنة النشر: | 2015 |
| المجموعة: | ScienceDirect (Elsevier - Open Access Articles via Crossref) |
| مصطلحات موضوعية: | Biochemistry (medical), Clinical Biochemistry, Biochemistry, General Medicine |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| DOI: | 10.1016/j.cca.2015.02.008 |
| الإتاحة: | https://doi.org/10.1016/j.cca.2015.02.008Test https://api.elsevier.com/content/article/PII:S0009898115000716?httpAccept=text/xmlTest https://api.elsevier.com/content/article/PII:S0009898115000716?httpAccept=text/plainTest |
| حقوق: | https://www.elsevier.com/tdm/userlicense/1.0Test/ |
| رقم الانضمام: | edsbas.6CFF06B7 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1016/j.cca.2015.02.008 |
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