Das Leben von Kindern mit der schweren angeborenen Immunschwäche X-SCID (X-chromosomal severe combined immunodeficiency) ist ständig bedroht, da ihr Immunsystem Infektionen mit Krankheitserregern nicht abwehren kann. Grund dafür ist ein Defekt im Gen für die gamma-Kette des Interleukin-2-Rezeptors (IL2RG).
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