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› A Novel Mutation of <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M1"><mml:mi>V</mml:mi><mml:mi>P</mml:mi><mml:mi>S</mml:mi><mml:mn>33</mml:mn><mml:mi>B</mml:mi></mml:math> Gene Associated with Incomplete Arthrogryposis-Renal Dysfunction-Cholestasis Phenotype
A Novel Mutation of <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M1"><mml:mi>V</mml:mi><mml:mi>P</mml:mi><mml:mi>S</mml:mi><mml:mn>33</mml:mn><mml:mi>B</mml:mi></mml:math> Gene Associated with Incomplete Arthrogryposis-Renal Dysfunction-Cholestasis Phenotype
Research article (Case Reports in Genetics, 2020) · cited 10× · AI/ML
A Novel Mutation of VPS33B Gene Associated with Incomplete Arthrogryposis-Renal Dysfunction-Cholestasis Phenotype
Summary
A Novel Mutation of VPS33B Gene Associated with Incomplete Arthrogryposis-Renal Dysfunction-Cholestasis Phenotype is a scholarly article[1].
Key Facts
A Novel Mutation of VPS33B Gene Associated with Incomplete Arthrogryposis-Renal Dysfunction-Cholestasis Phenotype's instance of is recorded as scholarly article[2].
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APA4ort.xyz Knowledge Graph. (2026). A Novel Mutation of <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" id="M1"><mml:mi>V</mml:mi><mml:mi>P</mml:mi><mml:mi>S</mml:mi><mml:mn>33</mml:mn><mml:mi>B</mml:mi></mml:math> Gene Associated with Incomplete Arthrogryposis-Renal Dysfunction-Cholestasis Phenotype. Retrieved May 24, 2026, from https://4ort.xyz/entity/a-novel-mutation-of-mml-math-xmlns-mml-http-www-w3-org-1998-math-mathml-id-m1-mml-mi-v-mml-mi-mml-mi-p-mml-mi-mml-mi-s-m
