Investigating Human VANGL1, as a Candidate Gene for Adolescent Idiopathic Scoliosis
Introduction The human VANGL1 genes has been predicted to be associated with idiopathic scoliosis, as a mutation (c.676C > T, L226F) was identified in a family with dominant inheritance of the disease. A previous investigation of the gene revealed the candidate to segregate, with all but one family...
محفوظ في:
| المؤلفون الرئيسيون: | , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
SAGE Publishing
2015-05-01
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| سلاسل: | Global Spine Journal |
| الوصول للمادة أونلاين: | https://doi.org/10.1055/s-0035-1554229 |
| الوسوم: |
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