Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q
| العنوان: | Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17q |
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| المؤلفون: | C. Van Broeckhoven, J. Meuleman, Vincent Timmerman, P. Spoelders, Eva Nelis, Manfred Wehnert |
| المصدر: | Neurology |
| بيانات النشر: | Ovid Technologies (Wolters Kluwer Health), 1997. |
| سنة النشر: | 1997 |
| مصطلحات موضوعية: | Adult, Genetic Markers, Male, Adolescent, Genetic Linkage, Pedigree chart, Hereditary neuralgic amyotrophy, medicine, Brachial Plexus Neuritis, Humans, Child, Family Health, Genetics, Linkage (software), business.industry, Infant, Chromosome, medicine.disease, Amyotrophy, Pedigree, Chromosome 17 (human), Child, Preschool, Female, Neurology (clinical), business, Neuroscience, Chromosomes, Human, Pair 17 |
| الوصف: | Hereditary neuralgic amyotrophy is a rare autosomal dominant disorder of the peripheral nervous system. Previous segregation analysis in two large pedigrees suggested linkage to distal 17q. Linkage data obtained in the present study investigating a three generation pedigree confirm linkage to 17q24-q25. |
| تدمد: | 1526-632X 0028-3878 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b4954208c99d7e0d93cb2a35f4b5766Test https://doi.org/10.1212/wnl.48.6.1719Test |
| حقوق: | CLOSED |
| رقم الانضمام: | edsair.doi.dedup.....4b4954208c99d7e0d93cb2a35f4b5766 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 1526632X 00283878 |
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