Anderson's disease/chylomicron retention disease in a...

Orphanet Journal of Rare Diseases 2011 / 12 Vol. 6; Iss. 1

Anderson's disease/chylomicron retention disease in a Japanese patient with uniparental disomy 7 and a normalSAR1Bgene protein coding sequence

Tomoo Okada, Michio Miyashita, Junji Fukuhara, Masahiko Sugitani, Takahiro Ueno, Marie-Elisabeth Samson-Bouma, Lawrence P Aggerbeck
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
6
Language:
english
DOI:
10.1186/1750-1172-6-78
Date:
December, 2011
File:
PDF, 824 KB
english, 2011
Conversion to is in progress
Conversion to is failed