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mouseMammal
alkaptonuriaDisease
Ochronotic osteoarthropathy in a mouse model of alkaptonuria, and its inhibition by nitisinon
Alkaptonuria (AKU) is a rare autosomal recessive disease, associated with deficiency of homogentisat...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive metabolic bone disease characterised by inc...
Question Does Nitisinone prevent the clinical progression of the Alkaptonuria? Findings In this obse...
Alkaptonuria (AKU) is a rare genetic disease resulting in severe, rapidly progressing, early onset m...
Alkaptonuria (AKU) is an ultrarare autosomal recessive disorder resulting from a deficiency of homog...
Purpose: Alkaptonuria is a rare autosomal recessive form of osteoarthropathy resulting from deficien...
SummaryObjectiveAlkaptonuria (AKU) is a rare genetic disease which results in severe early onset ost...
Alkaptonuria (AKU) is a rare multisystem metabolic disease caused by deficient activity of homogenti...
Introduction: Alkaptonuria is an iconic disease, dating back to the Egyptians and has continued to p...
Alkaptonuria (AKU) is an ultra rare autosomal recessive disorder resulting from a deficiency of the ...
OBJECTIVES: Alkaptonuria (AKU) is an orphan disease that has an estimated prevalence of 0.3/100,000....
Abstract Alkaptonuria (AKU, OMIM 203500) is a rare congenital disorder caused by a deficiency of the...
Background: Nitisinone-induced hypertyrosinaemia is well documented in Alkaptonuria (AKU), and there...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive disorder of tyrosine catabolism due to muta...
Alkaptonuria (AKU) is an ultra-rare genetic disease resulting from a lack in activity of the enzyme ...
Alkaptonuria (AKU) is a rare autosomal recessive disease, associated with deficiency of homogentisat...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive metabolic bone disease characterised by inc...
Question Does Nitisinone prevent the clinical progression of the Alkaptonuria? Findings In this obse...
Alkaptonuria (AKU) is a rare genetic disease resulting in severe, rapidly progressing, early onset m...
Alkaptonuria (AKU) is an ultrarare autosomal recessive disorder resulting from a deficiency of homog...
Purpose: Alkaptonuria is a rare autosomal recessive form of osteoarthropathy resulting from deficien...
SummaryObjectiveAlkaptonuria (AKU) is a rare genetic disease which results in severe early onset ost...
Alkaptonuria (AKU) is a rare multisystem metabolic disease caused by deficient activity of homogenti...
Introduction: Alkaptonuria is an iconic disease, dating back to the Egyptians and has continued to p...
Alkaptonuria (AKU) is an ultra rare autosomal recessive disorder resulting from a deficiency of the ...
OBJECTIVES: Alkaptonuria (AKU) is an orphan disease that has an estimated prevalence of 0.3/100,000....
Abstract Alkaptonuria (AKU, OMIM 203500) is a rare congenital disorder caused by a deficiency of the...
Background: Nitisinone-induced hypertyrosinaemia is well documented in Alkaptonuria (AKU), and there...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive disorder of tyrosine catabolism due to muta...
Alkaptonuria (AKU) is an ultra-rare genetic disease resulting from a lack in activity of the enzyme ...
Alkaptonuria (AKU) is a rare autosomal recessive disease, associated with deficiency of homogentisat...
Alkaptonuria (AKU) is an ultra-rare, autosomal recessive metabolic bone disease characterised by inc...
Question Does Nitisinone prevent the clinical progression of the Alkaptonuria? Findings In this obse...
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