Musialik, J.; Boguszewska-Chachulska, A.; Pojda-Wilczek, D.; Gorzkowska, A.; Szymańczak, R.; Kania, M.; Kujawa-Szewieczek, A.; Wojcieszyn, M.; Hartleb, M.; Więcek, A.
A Rare Mutation in The APOB Gene Associated with Neurological Manifestations in Familial Hypobetalipoproteinemia. Int. J. Mol. Sci. 2020, 21, 1439.
https://doi.org/10.3390/ijms21041439
AMA Style
Musialik J, Boguszewska-Chachulska A, Pojda-Wilczek D, Gorzkowska A, Szymańczak R, Kania M, Kujawa-Szewieczek A, Wojcieszyn M, Hartleb M, Więcek A.
A Rare Mutation in The APOB Gene Associated with Neurological Manifestations in Familial Hypobetalipoproteinemia. International Journal of Molecular Sciences. 2020; 21(4):1439.
https://doi.org/10.3390/ijms21041439
Chicago/Turabian Style
Musialik, Joanna, Anna Boguszewska-Chachulska, Dorota Pojda-Wilczek, Agnieszka Gorzkowska, Robert Szymańczak, Magdalena Kania, Agata Kujawa-Szewieczek, Małgorzata Wojcieszyn, Marek Hartleb, and Andrzej Więcek.
2020. "A Rare Mutation in The APOB Gene Associated with Neurological Manifestations in Familial Hypobetalipoproteinemia" International Journal of Molecular Sciences 21, no. 4: 1439.
https://doi.org/10.3390/ijms21041439
APA Style
Musialik, J., Boguszewska-Chachulska, A., Pojda-Wilczek, D., Gorzkowska, A., Szymańczak, R., Kania, M., Kujawa-Szewieczek, A., Wojcieszyn, M., Hartleb, M., & Więcek, A.
(2020). A Rare Mutation in The APOB Gene Associated with Neurological Manifestations in Familial Hypobetalipoproteinemia. International Journal of Molecular Sciences, 21(4), 1439.
https://doi.org/10.3390/ijms21041439
