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Fig. 1 | BMC Medical Genetics

Fig. 1

From: Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease

Fig. 1

Schematic representation of fibrocystin with indicated localization of mutations detected in our study. Protein domains: green – extracellular domain, pink – transmembrane domain, violet – intracellular domain. The number of occurrence is shown for recurrent mutations. Missense mutations are shown in blue, truncating mutations in red [33]

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