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Fig. 1 | BMC Medical Genetics

Fig. 1

From: Isolated hypoaldosteronism as first sign of X-linked adrenal hypoplasia congenita caused by a novel mutation in NR0B1/DAX-1 gene: a case report

Fig. 1

Partial chromatograms showing the novel NR0B1 /DAX-1 mutation. Base change c.848_849delinsCC leading to the missense mutation p.(Gln283Pro). The reference sequence is in highlighted in red. The proband’s DNA sequence is above, the mother’s DNA sequence in the middle and a healthy control’s sequence underneath

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BMC Medical Genetics

ISSN: 1471-2350

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