A novel frame-shift deletion in FANCF gene causing...

BMC Medical Genetics 2019 / 12 Vol. 20; Iss. 1

A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report

Zareifar, Soheila, Dastsooz, Hassan, Shahriari, Mahdi, Faghihi, Mohammad Ali, Shekarkhar, Golsa, Bordbar, Mohammadreza, Zekavat, Omid Reza, Shakibazad, Nader
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Volume:
20
Language:
english
Journal:
BMC Medical Genetics
DOI:
10.1186/s12881-019-0855-2
Date:
December, 2019
File:
PDF, 2.66 MB
english, 2019
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