دورية أكاديمية
Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case report
العنوان: | Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case report |
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المؤلفون: | Simoes, CamilaAff1, Aff2, Graña, Martín, Rodriguez, Soledad, Baltar Yanes, Federico, Tapié, Alejandra, Dell’Oca, Nicolás, Naya, HugoAff1, Aff5, Raggio, Víctor, Spangenberg, LucíaAff1, Aff6, IDs12887022035956_cor9 |
المصدر: | BMC Pediatrics. 22(1) |
قاعدة البيانات: | Springer Nature Journals |
تدمد: | 14712431 |
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DOI: | 10.1186/s12887-022-03595-6 |