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Anderson’s disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities

✍ Scribed by M Silvain; D Bligny; T Aparicio; P Laforêt; A Grodet; N Peretti; D Ménard; F Djouadi; C Jardel; JM Bégué; F Walker; J Schmitz; A Lachaux; LP Aggerbeck; ME Samson-Bouma


Book ID
110888671
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
176 KB
Volume
74
Category
Article
ISSN
0009-9163

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