| 1. | The FANCG gene is responsible for complementation group G.
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| 2. | This gene encodes the protein for complementation group E.
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| 3. | The clinical phenotype of all Fanconi anemia ( FA ) complementation groups is similar.
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| 4. | These patients are classified as XP complementation group F ( XP-F ).
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| 5. | This gene encodes a member of the Fanconi anemia, complementation group A protein.
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| 6. | GSTP1 has been shown to interact with Fanconi anemia, complementation group C and MAPK8.
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| 7. | The clinical phenotype of mutational defects in all Fanconi anemia ( FA ) complementation groups is similar.
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| 8. | FA patients with ERCC4 mutations have been classified as belonging to Fanconi anemia complementation group P ( FANCP ).
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| 9. | FANCF has been shown to interact with Fanconi anemia, complementation group C, FANCG, FANCA and FANCE.
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| 10. | This gene encodes the protein for complementation group I . Alternative splicing results in two transcript variants encoding different isoforms.
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