APA

Silvain M., Bligny D., Aparicio T., Laforêt P., Grodet A., Peretti N., Ménard D., Djouadi F., Jardel C., Bégué J. M., Walker F., Schmitz J., Lachaux A., Aggerbeck L. P. & Samson-Bouma M. E. (20090204). Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities. : Clinical genetics.

Chicago

Silvain M, Bligny D, Aparicio T, Laforêt P, Grodet A, Peretti N, Ménard D, Djouadi F, Jardel C, Bégué J M, Walker F, Schmitz J, Lachaux A, Aggerbeck L P and Samson-Bouma M E. 20090204. Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities. : Clinical genetics.

Harvard

Silvain M., Bligny D., Aparicio T., Laforêt P., Grodet A., Peretti N., Ménard D., Djouadi F., Jardel C., Bégué J. M., Walker F., Schmitz J., Lachaux A., Aggerbeck L. P. and Samson-Bouma M. E. (20090204). Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities. : Clinical genetics.

MLA

Silvain M, Bligny D, Aparicio T, Laforêt P, Grodet A, Peretti N, Ménard D, Djouadi F, Jardel C, Bégué J M, Walker F, Schmitz J, Lachaux A, Aggerbeck L P and Samson-Bouma M E. Anderson's disease (chylomicron retention disease): a new mutation in the SARA2 gene associated with muscular and cardiac abnormalities. : Clinical genetics. 20090204.