Add to ORKGAdenine phosphoribosyltransferase (APRT) deficiency: a new genetic mutation with early recurrent renal stone disease in kidney transplantatio
Inherited metabolic diseases resulting in urolithiasis secondary to urinary excretion of insoluble s...
Complete adenine phosphoribosyl transferase (APRT) deficiency is a rare inherited metabolic disorder...
Adenine phosphoribosyltransferase (APRT) deficiency, cystinuria, Dent disease, familial hypomagnesem...
APRT deficiency is a rare but under recognized genetic disease. Recurrent urolithiasis and DHA ...
Adenine phosphoribosyltransferase (APRT) enzyme deficiency is an important and potentially reversibl...
Adenine phosphoribosyltransferase (APRT) deficiency is an autosomal recessive purine enzyme defect ...
To access publisher's full text version of this article, please click on the hyperlink in Additional...
Adenine phosphoribosyltransferase (APRT) catalyzes the synthesis of AMP from adenine and 5-phosphori...
Item does not contain fulltextWe have examined the mutational basis of adenine phosphoribosyltransfe...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive enzyme defect of p...
Publisher Copyright: © 2021, The Author(s), under exclusive licence to European Society of Human Gen...
We describe a family of Turkish origin with adenine phosphoribosyltransferase (APRT) deficiency and ...
To access publisher's full text version of this article click on the hyperlink belowAdenine phosphor...
A 30-year-old woman with history of passage of stones since childhood presented with oliguria and pe...
Inherited metabolic diseases resulting in urolithiasis secondary to urinary excretion of insoluble s...
Complete adenine phosphoribosyl transferase (APRT) deficiency is a rare inherited metabolic disorder...
Adenine phosphoribosyltransferase (APRT) deficiency, cystinuria, Dent disease, familial hypomagnesem...
APRT deficiency is a rare but under recognized genetic disease. Recurrent urolithiasis and DHA ...
Adenine phosphoribosyltransferase (APRT) enzyme deficiency is an important and potentially reversibl...
Adenine phosphoribosyltransferase (APRT) deficiency is an autosomal recessive purine enzyme defect ...
To access publisher's full text version of this article, please click on the hyperlink in Additional...
Adenine phosphoribosyltransferase (APRT) catalyzes the synthesis of AMP from adenine and 5-phosphori...
Item does not contain fulltextWe have examined the mutational basis of adenine phosphoribosyltransfe...
To access publisher's full text version of this article click on the hyperlink at the bottom of the ...
Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive enzyme defect of p...
Publisher Copyright: © 2021, The Author(s), under exclusive licence to European Society of Human Gen...
We describe a family of Turkish origin with adenine phosphoribosyltransferase (APRT) deficiency and ...
To access publisher's full text version of this article click on the hyperlink belowAdenine phosphor...
A 30-year-old woman with history of passage of stones since childhood presented with oliguria and pe...
Inherited metabolic diseases resulting in urolithiasis secondary to urinary excretion of insoluble s...
Complete adenine phosphoribosyl transferase (APRT) deficiency is a rare inherited metabolic disorder...
Adenine phosphoribosyltransferase (APRT) deficiency, cystinuria, Dent disease, familial hypomagnesem...