| Entry |
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| Name |
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| Gene |
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| Organism |
hsa_var Human gene variants (Homo sapiens)
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| Variation |
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| Network |
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| Disease |
| H00106 | Complement regulatory protein defects |
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| Reference |
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| Authors |
Motoyama N, Okada N, Yamashina M, Okada H |
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| Title |
Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene. |
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| Journal |
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| LinkDB |
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