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Fig. 2 | BMC Pediatrics

Fig. 2

From: A novel variant of DNM1L expanding the clinical phenotypic spectrum: a case report and literature review

Fig. 2

Genetic location of DNM1L gene variants associated with mitochondrial diseases identified to date. A Schematic representation of the location of identified variants in each domain of the DRP1 protein. Changes in amino acid distribution associated with protein domains. Variants reported in this study are shown in red, and “x” indicates the number of cases. B The number of previously reported variants in each domain. C Comparison of the amino acid sequences of the DRP1 protein in different species. The amino acid sequence of the variant site is highly conserved (red font)

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BMC Pediatrics

ISSN: 1471-2431

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