دورية أكاديمية
SMN gene deletion in variant of infantile spinal muscular atrophy.
العنوان: | SMN gene deletion in variant of infantile spinal muscular atrophy. |
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المؤلفون: | Bürglen, L.1,2,3,4, Spiegel, R.1,2,3,4, Ignatius, J.1,2,3,4, Cobben, J. M.1,2,3,4, Landrieu, P.1,2,3,4, Lefebvre, S.1,2,3,4, Munnich, A.1,2,3,4, Melki, J.5 |
المصدر: | Lancet. 7/29/1995, Vol. 346 Issue 8970, p316-317. 2p. |
مصطلحات موضوعية: | CHROMOSOMES, CONGENITAL heart disease, GENETICS, MUSCULAR atrophy, GENETIC mutation, GENOTYPES |
قاعدة البيانات: | Business Source Index |
تدمد: | 01406736 |
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DOI: | 10.1016/s0140-6736(95)92206-7 |