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Fig. 2 | Hereditas

Fig. 2

From: Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes

Fig. 2

Pedigree connecting families with LQTS and HH to a common founder couple b 1614/1605. IV:1 is identical to AJ b 1694 from Fig. 1 and V:3-V4 b 1729 /1727 were her neighbors . Double heterozygotes (LQT/HFE) are marked by lower arrows. XII:12 ,marked by a lower left arrow, had a hearing aid at age 42. Symbols as in Fig. 1

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Hereditas

ISSN: 1601-5223

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