A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation
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F. Alkuraya | K. Khabar | Arif O. Khan | M. Al-Saif | M. Abouelhoda | N. Patel | N. Ibrahim | M. Hashem | F. Abdulwahab | W. Moghrabi | Tarfa Alshidi | Rana Alomar | Eman Alobeid | Balsam M. AlMaarik | Saad Al-Harbi