A case of Dunnigan-type familial partial lipodystrophy (FPLD) due to lamin A/C ( LMNA ) mutations complicated by end-stage renal disease

Verfasser / Beitragende:
[Hitomi Imachi, Koji Murao, Shouji Ohtsuka, Mako Fujiwara, Tomie Muraoka, Hitoshi Hosokawa, Toshihiko Ishida]
Ort, Verlag, Jahr:
2009
Enthalten in:
Endocrine, 35/1(2009-02-01), 18-21
Format:
Artikel (online)
ID: 453622097