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Fig. 2 | BMC Pediatrics

Fig. 2

From: CD40LG-associated X-linked Hyper-IgM Syndrome (XHIGM) with pulmonary alveolar proteinosis: a case report

Fig. 2

Electropherograms for the Sanger sequencing and schematic diagram of CD40LG. (A) The sequencing electropherograms indicate that the mutation c.516T > A is from the patient’s mother. (B) The intracellular domain (IC), trans-membrane domain (TM), extracellular unique domain (EU), and extracellular tumor necrosis factor homology domain of CD40LG are presented in the image. All affected residues/nucleotides in individuals with XHIGM with PAP were located within the TNFH domain

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BMC Pediatrics

ISSN: 1471-2431

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