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

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YILMAZ B., KOR D., Mungan N., ERDEM S., CEYLANER S.

Journal of pediatric endocrinology & metabolism : JPEM, vol.28, pp.1179-81, 2015 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 28
• Publication Date: 2015
• Doi Number: 10.1515/jpem-2014-0528
• Journal Name: Journal of pediatric endocrinology & metabolism : JPEM
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.1179-81
• Çukurova University Affiliated: Yes