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Inactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia

Document Type

Article

Author

Zagnoli-Vieira, G.; Brazina, J.; Caldecott, K.W.; Van Den Bogaert, K.; Huybrechts, W.; Van Esch, H.; Molenaers, G.

Source

In: Human Genetics. (Human Genetics, September 2023, 142(9):1417-1427)

Subject

Language

English

ISSN

14321203
03406717

Online Access

Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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