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ATP6V1B1 gene

Known as: ATP6V1B1, Vma2, ATP6B1 
National Institutes of Health

Papers overview

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Highly Cited
2016
Highly Cited
2016
Hearing impairment is the most frequent sensory deficit in humans. Deafness genes, which harbor pathogenic mutations that have… 
2015
2015
Autosomal recessive distal renal tubular acidosis (dRTA) is associated with mutation in the ATP6B1 gene encoding the B1 subunit… 
2015
2015
Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA Introduction: PIK3CA mutation has been becoming… 
Highly Cited
2003
Highly Cited
2003
Abstract.Primary distal renal tubular acidosis (dRTA) type I is a hereditary renal tubular disorder, which is characterized by… 
2003
2003
A large proportion of autosomal recessive distal renal tubular acidosis (RTA) is associated with mutations in the ATP6B1 gene… 
2000
2000
Distal renal tubular acidosis is characterized by an impaired H(+)-ion secretion in the distal tubulus. This may cause metabolic… 
2000
2000
ZusammenfassungBei der distalen renalen tubulären Azidose (drtA) ist die H+-Ionensekretion des distalen Tubulus gestört. Hieraus…