APA

Baumann M., Steichen-Gersdorf E., Krabichler B., Petersen B., Weber U., Schmidt W. M., Zschocke J., Müller T., Bittner R. E. & Janecke A. R. (20170705). Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype-phenotype correlation. : European journal of human genetics : EJHG.

Chicago

Baumann Matthias, Steichen-Gersdorf Elisabeth, Krabichler Birgit, Petersen Britt-Sabina, Weber Ulrike, Schmidt Wolfgang M, Zschocke Johannes, Müller Thomas, Bittner Reginald E and Janecke Andreas R. 20170705. Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype-phenotype correlation. : European journal of human genetics : EJHG.

Harvard

Baumann M., Steichen-Gersdorf E., Krabichler B., Petersen B., Weber U., Schmidt W. M., Zschocke J., Müller T., Bittner R. E. and Janecke A. R. (20170705). Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype-phenotype correlation. : European journal of human genetics : EJHG.

MLA

Baumann Matthias, Steichen-Gersdorf Elisabeth, Krabichler Birgit, Petersen Britt-Sabina, Weber Ulrike, Schmidt Wolfgang M, Zschocke Johannes, Müller Thomas, Bittner Reginald E and Janecke Andreas R. Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype-phenotype correlation. : European journal of human genetics : EJHG. 20170705.