APA
Baumann M., Giunta C., Krabichler B., Rüschendorf F., Zoppi N., Colombi M., Bittner R. E., Quijano-Roy S., Muntoni F., Cirak S., Schreiber G., Zou Y., Hu Y., Romero N. B., Carlier R. Y., Amberger A., Deutschmann A., Straub V., Rohrbach M., Steinmann B., Rostásy K., Karall D., Bönnemann C. G., Zschocke J. & Fauth C. (20120619). Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss. : American journal of human genetics.
Chicago
Baumann Matthias, Giunta Cecilia, Krabichler Birgit, Rüschendorf Franz, Zoppi Nicoletta, Colombi Marina, Bittner Reginald E, Quijano-Roy Susana, Muntoni Francesco, Cirak Sebahattin, Schreiber Gudrun, Zou Yaqun, Hu Ying, Romero Norma Beatriz, Carlier Robert Yves, Amberger Albert, Deutschmann Andrea, Straub Volker, Rohrbach Marianne, Steinmann Beat, Rostásy Kevin, Karall Daniela, Bönnemann Carsten G, Zschocke Johannes and Fauth Christine. 20120619. Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss. : American journal of human genetics.
Harvard
Baumann M., Giunta C., Krabichler B., Rüschendorf F., Zoppi N., Colombi M., Bittner R. E., Quijano-Roy S., Muntoni F., Cirak S., Schreiber G., Zou Y., Hu Y., Romero N. B., Carlier R. Y., Amberger A., Deutschmann A., Straub V., Rohrbach M., Steinmann B., Rostásy K., Karall D., Bönnemann C. G., Zschocke J. and Fauth C. (20120619). Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss. : American journal of human genetics.
MLA
Baumann Matthias, Giunta Cecilia, Krabichler Birgit, Rüschendorf Franz, Zoppi Nicoletta, Colombi Marina, Bittner Reginald E, Quijano-Roy Susana, Muntoni Francesco, Cirak Sebahattin, Schreiber Gudrun, Zou Yaqun, Hu Ying, Romero Norma Beatriz, Carlier Robert Yves, Amberger Albert, Deutschmann Andrea, Straub Volker, Rohrbach Marianne, Steinmann Beat, Rostásy Kevin, Karall Daniela, Bönnemann Carsten G, Zschocke Johannes and Fauth Christine. Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss. : American journal of human genetics. 20120619.