小说FERMT3和PTPRQ与白细胞粘附性缺陷-III和感觉神经听力损失相关的突变

Gabriela de Toledo Passos Candelaria1, Alexandre de A Antunes1, Antonio C Pastorino2

  • 1Department of Pediatrics, Hematology-Oncology Service, Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil.

PubMed
概括

这项研究确定了FERMT3和PTPRQ基因在患有白细胞粘附性缺陷-III和神经感官听力损失的患者中的新突变. 这些发现促进了对罕见遗传疾病及其基因型-表型相关性的理解.

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