Sporadic  TP63  gene mutation with primary T-cell immunodeficiency and previously undescribed genetic site mutation (GERP++): case report

Amanzhan S. Aldan’yazov; Alina K. Makenova; Anastasiya N. Yakovlevna; Anastasiya A. Truhanova

Sporadic TP63 gene mutation with primary T-cell immunodeficiency and previously undescribed genetic site mutation (GERP++): case report

Amanzhan S. Aldan’yazov, Alina K. Makenova, Anastasiya N. Yakovlevna, Anastasiya A. Truhanova

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About the Authors

Amanzhan S. Aldan’yazov

ФГБОУ ВО ОрГМУ
Russian Federation

Alina K. Makenova

ФГБОУ ВО ОрГМУ
Russian Federation

Anastasiya N. Yakovlevna

ФГБОУ ВО ОрГМУ
Russian Federation

Anastasiya A. Truhanova

ФГБОУ ВО ОрГМУ
Russian Federation

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Aldan’yazov A.S., Makenova A.K., Yakovlevna A.N., Truhanova A.A. Sporadic TP63 gene mutation with primary T-cell immunodeficiency and previously undescribed genetic site mutation (GERP++): case report. Russian Pediatric Journal. 2025;6(1):34. (In Russ.)

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ISSN 2687-0843 (Online)

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Russian Pediatric Journal

Sporadic TP63 gene mutation with primary T-cell immunodeficiency and previously undescribed genetic site mutation (GERP++): case report

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