- Title
- A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report
- Creators
- Soheila Zareifar - Shiraz, IranHassan Dastsooz - Turin, ItalyMahdi Shahriari - Shiraz, IranMohammad Ali Faghihi - Miami, USAGolsa Shekarkhar - Shiraz, IranMohammadreza Bordbar - Shiraz, IranOmid Reza Zekavat - Shiraz, IranNader Shakibazad - Shiraz, Iran
- Publication Details
- BMC medical genetics, Vol.20(1), pp.122-122
- Publisher
- BioMed Central; London
- Academic Unit
- Miller School of Medicine; UMMG Dept of Psychiatry & Behavioral Sciences
- Language
- English
- Resource Type
- Journal article
- PMID
- 31288759
- PMCID
- PMC6617641
- Record Identifier
- 991031576474902976
Journal article
A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case report
BMC medical genetics, Vol.20(1), pp.122-122
2019-07-09
PMCID: PMC6617641
PMID: 31288759
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13 Record Views
InCites Highlights
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- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.152 Molecular & Cell Biology - DNA Damage
- 1.152.257 DSBs
- Web Of Science research areas
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
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Source: InCites