| 1 |
Review on Spinal Muscular Atrophy |
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| Omkar A. Devade, Rohan D. Londhe, Nikhil M. Meshram |
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Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran |
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| Zohreh Sharifi, Mohammad Taheri, Mohammad-Sadegh Fallah, Maryam Abiri, Fatemeh Golnabi, Hamideh Bagherian, Razieh Zeinali, Hossein Farahzadi, Marjan Alborji, Pardis Ghazizadeh Tehrani, Masoume Amini, Sadaf Asnavandi, Mehrdad Hashemi, Flora Forouzesh, Sirous Zeinali |
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Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy |
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| Rekik, I. and Boukhris, A. and Ketata, S. and Amri, M. and Essid, N. and Feki, I. and Mhiri, C. |
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| Annals of Indian Academy of Neurology. 2013; 16(1): 57-61 |
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Correlation between deletion patterns of SMN1 and NAIP genes and clinical subtypes of spinal muscular atrophy in Iranian Azeri Turk ethnic patients |
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| Barzegar, M. and Shiva, S. and Bonyadi, M.J. and Toopchizadeh, V. |
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Isolated exon 8 deletion in type 1 spinal muscular atrophy with bilateral optic atrophy: Unusual genetic mutation leading to unusual manifestation? |
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| Maiti, D. and Bhattacharya, M. and Yadav, S. |
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Autosomal dominant Late-onset Quadriceps Myopathy: Three Patients of a Taiwanese Kindred |
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| Yu-Yi Chien, Ikuya Nonaka, Daryi Wang |
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Deletion analysis of SMN1 and NAIP genes in southern Chinese children with spinal muscular atrophy |
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| Yu-hua Liang, Xiao-ling Chen, Zhong-sheng Yu, Chun-yue Chen, Sheng Bi, Lian-gen Mao, Bo-lin Zhou, Xian-ning Zhang |
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Possible association between L-selectin gene P213S polymorphism and respiratory complications of childhood spinal muscular atrophy patients |
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| Stavarachi, M., Apostol, P., Cimponeriu, D., Toma, M., Butoianu, N., Gavrilǎ, L. |
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Limb girdle muscular dystrophies in India |
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| Khadilkar, S., Singh, R. |
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Deletion analysis of spinal muscular atrophy in southern Indian population |
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| Singh, R. |
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