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ATP6AP1‐CDG: Follow‐up and female phenotype
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ATP6AP1‐CDG: Follow‐up and female phenotype
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JIMD Reports
ATP6AP1‐CDG: Follow‐up and female phenotype
DOI:
10.1002/jmd2.12104, Volume: 53, Issue: 1, Pages: 80-82
Article Type:
research-article,
Article History
received:
2019-12-3
rev-recd:
2020-2-3
accepted:
2020-2-6
published:
2020-5-9
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Keywords
Proteinuria
,
ATP6AP1 deficiency
,
congenital disorder of glycosylation
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https://www.researchpad.co/tools/openurl?pubtype=&doi=10.1002/jmd2.12104&title=ATP6AP1‐CDG: Follow‐up and female phenotype&author=&keyword=[{keywordId=7491, uniqueName=proteinuria, name=Proteinuria, contentId=9555}, {keywordId=9798, uniqueName=atp6ap1-deficiency, name=ATP6AP1 deficiency, contentId=9555}, {keywordId=9799, uniqueName=congenital-disorder-of-glycosylation, last=true, name=congenital disorder of glycosylation, contentId=9555}],[{keywordId=7491, uniqueName=proteinuria, name=Proteinuria, contentId=9555}, {keywordId=9798, uniqueName=atp6ap1-deficiency, name=ATP6AP1 deficiency, contentId=9555}, {keywordId=9799, uniqueName=congenital-disorder-of-glycosylation, last=true, name=congenital disorder of glycosylation, contentId=9555}],[{keywordId=7491, uniqueName=proteinuria, name=Proteinuria, contentId=9555}, {keywordId=9798, uniqueName=atp6ap1-deficiency, name=ATP6AP1 deficiency, contentId=9555}, {keywordId=9799, uniqueName=congenital-disorder-of-glycosylation, last=true, name=congenital disorder of glycosylation, contentId=9555}],&subject=
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