Mutations in TTC21B cause different phenotypes in two childhood cases in China
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DOI: 10.1111/nep.13008
Abstract: The TTC21B gene is now known as causative of nephronophthisis‐related ciliopathies (NPHP‐RC). We reported two Chinese paediatric cases with end‐stage renal disease and other phenotypes caused by the TTC21B gene mutations. read more here.
Keywords: cause different; two childhood; mutations ttc21b; ttc21b cause ... See more keywords