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

✍ Scribed by Hitomi Imachi; Koji Murao; Shouji Ohtsuka; Mako Fujiwara; Tomie Muraoka; Hitoshi Hosokawa; Toshihiko Ishida


Book ID
107571231
Publisher
Springer
Year
2008
Tongue
English
Weight
202 KB
Volume
35
Category
Article
ISSN
0969-711X

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