Distal renal tubular acidosis caused by tryptophan‐aspartate repeat domain 72 (WDR72) mutations

N Rungroj, C Nettuwakul, N Sawasdee… - Clinical …, 2018 - Wiley Online Library
Hereditary distal renal tubular acidosis (dRTA) is a rare genetic disease that is caused by
mutations in SLC4A1, ATP6V1B1, or ATP6V0A4. However, there are many families with …
被引用次数：70 相关文章

Distal renal tubular acidosis caused by tryptophan‐aspartate repeat domain 72 (WDR72) mutations.

N Rungroj, C Nettuwakul, N Sawasdee… - Clinical …, 2018 - search.ebscohost.com
Hereditary distal renal tubular acidosis (dRTA) is a rare genetic disease that is caused by
mutations in SLC4A1, ATP6V1B1, or ATP6V0A4. However, there are many families with …

Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations

N Rungroj, C Nettuwakul, N Sawasdee… - Clinical …, 2018 - pubmed.ncbi.nlm.nih.gov
Hereditary distal renal tubular acidosis (dRTA) is a rare genetic disease that is caused by
mutations in SLC4A1, ATP6V1B1, or ATP6V0A4. However, there are many families with …

Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations

N Rungroj, C Nettuwakul, N Sawasdee… - Clinical …, 2018 - mahidol.elsevierpure.com
Hereditary distal renal tubular acidosis (dRTA) is a rare genetic disease that is caused by
mutations in SLC4A1, ATP6V1B1, or ATP6V0A4. However, there are many families with …

Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations.

N Rungroj, C Nettuwakul, N Sawasdee… - Clinical …, 2018 - europepmc.org
Hereditary distal renal tubular acidosis (dRTA) is a rare genetic disease that is caused by
mutations in SLC4A1, ATP6V1B1, or ATP6V0A4. However, there are many families with …