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Fig. 2 | BMC Neurology

Fig. 2

From: Co-occurrence of Moyamoya syndrome and Kartagener syndrome caused by the mutation of DNAH5 and DNAH11: a case report

Fig. 2

Co-occurrence of moyamoya syndrome and Kartagener syndrome associated with mutations in DNAH5 and DNAH11 gene. The whole genome sequencing analysis showed a nonsense mutation c.9286C > T (p.Arg3096Ter) in the DNAH5 gene (a) and heterozygotic missense mutation including c.73G > A (p.Ala25Thr) and c.5702A > C (p.Glu1901Ala) in the DNAH11 gene (b)

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BMC Neurology

ISSN: 1471-2377

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