机译:单一的干扰素:蜡烛综合征的表型和基因型发现及其与C1Q缺陷的重叠。
Department of Pediatric RheumatologyKing Faisal Specialist Hospital and Research CenterRiyadh Saudi;
Department of Pediatric RheumatologyKing Faisal Specialist Hospital and Research CenterRiyadh Saudi;
Department of Pediatric RheumatologyKing Faisal Specialist Hospital and Research CenterRiyadh Saudi;
Department of Pediatric RheumatologyKing Faisal Specialist Hospital and Research CenterRiyadh Saudi;
Department of PathologyKing Faisal Specialist Hospital and Research CenterRiyadh Saudi Arabia;
Department of GeneticsKing Faisal Specialist Hospital and Research CenterRiyadh Saudi Arabia;
Department of Allergy and ImmunologyKing Faisal Specialist Hospital and Research CenterRiyadh Saudi;
CANDLE syndrome; C1q deficiency; systemic lupus erythematosus; autoinflammatory; interferonopathies;
机译:单一的干扰素:蜡烛综合征的表型和基因型发现及其与C1Q缺陷的重叠。
机译:孟德尔干扰神经病的见解:CANDLE,SAVI与AGS,单基因狼疮的比较
机译:SCN4A变体和Brugada综合征:心脏和骨骼肌钠通道病之间的表型和基因型重叠
机译:日本KCJVJ2相关anderen-tawils综合征的基因型/表型特征
机译:孟德尔干扰神经病的见解:CANDLESAVI与AGS单基因狼疮的比较
机译:SCN4A变异和Brugada综合征:心肌和骨骼肌钠通道病之间的表型和基因型重叠