Primary systemic carnitine deficiency: a Turkish case with...

Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up

Yilmaz, Berna Seker, Kor, Deniz, Mungan, Neslihan Onenli, Erdem, Sevcan, Ceylaner, Serdar
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Volume:
28
Language:
english
Journal:
Journal of Pediatric Endocrinology and Metabolism
DOI:
10.1515/jpem-2014-0528
Date:
January, 2015
File:
PDF, 531 KB
english, 2015
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