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. Author manuscript; available in PMC: 2020 Aug 5.
Published in final edited form as: J Med Genet. 2019 Oct 5;57(4):274–282. doi: 10.1136/jmedgenet-2019-106409

Figure 1. Consanguineous families with a homozygous recessive mutation in TMX2.

Figure 1.

(A-D) Pedigrees of all four families showing first-cousin consanguineous marriages (double bar) with a total of eight affected children. All unfilled members are without neurological disease.