Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation
Abstract Background Acute respiratory distress syndrome (ARDS) causes significant mortality in young children with certain diseases. Early diagnosis and treatment can reduce infant mortality. Here, we report a rare case of exome sequencing in the early diagnosis of immunodeficiency in an infant. Cas...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2022-07-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |