Rapid whole‐genome sequencing leading to specific treatment for two infants with haemophagocytic lymphohistiocytosis due to Wolman disease.

Autor: Selvanathan, Arthavan, Forwood, C., Russell, J., Batten, K., Thompson, S., Palmer, E. E., Macintosh, R., Nightingale, S., Mitchell, R., Alvaro, F., Dudding‐Byth, T., Lunke, S., Christodoulou, J., Stark, Z., White, F., Jones, S. A., Bhattacharya, K.
Zdroj: Pediatric Blood & Cancer; Sep2023, Vol. 70 Issue 9, p1-4, 4p
Databáze: Complementary Index
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