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Fig. 2 | Journal of Medical Case Reports

Fig. 2

From: Wolman disease presenting with hemophagocytic lymphohistiocytosis syndrome and a novel LIPA gene variant: a case report and review of the literature 

Fig. 2

An electropherogram of father (top), mother (second), patient (third), and control (bottom), demonstrates a mutation (arrow) in exon 4 that results in conversion of amino acid glycine at position 118 to aspartic acid. On the top, the arrow indicates the paternally inherited c.482delA and the arrow in the second row approximates the location of the maternally inherited deletion

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Journal of Medical Case Reports

ISSN: 1752-1947