Familial Partial Lipodystrophy Caused by a Novel Lamin A/C (LMNA) Mutation in Exon 1 (D47N)


ÖZDEMİR KUTBAY N., ŞARER YÜREKLİ B. P., Onay H., Altay C. T., ATİK T., HEKİMSOY Z., ...More

Bridging the World of Endocrinology, Antalya, Turkey, 15 - 18 October 2015, (Summary Text)

  • Publication Type: Conference Paper / Summary Text
  • City: Antalya
  • Country: Turkey
  • Manisa Celal Bayar University Affiliated: Yes