Fanconi anemia and βc deficiency-associated pulmonary alveolar proteinosis as two hereditary diseases of childhood which are potentially curable by stem cell gene therapy but require different therapeutic approaches.
| Autor: | Dirksen, U., Moritz, T., Burdach, S., Flasshove, M., Hanenberg, H. |
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| Zdroj: | Klinische Pädiatrie; 1999, Vol. 211 Issue 4, p329-335, 7p |
| Databáze: | Complementary Index |
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