A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephaly

MLA

Annemarie Haeberli, et al. “A Novel Mutation in BCS1L Associated with Deafness, Tubulopathy, Growth Retardation and Microcephaly.” European Journal of Pediatrics, vol. 175, Nov. 2015, pp. 517–25. EBSCOhost, https://doi.org/10.1007/s00431-015-2661-y.

APA

Annemarie Haeberli, Alessandra Ferrarini, Luisa Bonafé, Jean-Marc Nuoffer, André Schaller, Sabina Gallati, M F Bauer, Hassib Chehade, Frédéric Barbey, Christel Tran, Christopher B. Jackson, Dagmar Hahn, Sandra Eggimann, & Urania Kotzaeridou. (2015). A novel mutation in BCS1L associated with deafness, tubulopathy, growth retardation and microcephaly. European Journal of Pediatrics, 175, 517–525. https://doi.org/10.1007/s00431-015-2661-y

Chicago

Annemarie Haeberli, Alessandra Ferrarini, Luisa Bonafé, Jean-Marc Nuoffer, André Schaller, Sabina Gallati, M F Bauer, et al. 2015. “A Novel Mutation in BCS1L Associated with Deafness, Tubulopathy, Growth Retardation and Microcephaly.” European Journal of Pediatrics 175 (November): 517–25. doi:10.1007/s00431-015-2661-y.