A novel variant in the COL6A1 gene causing Ullrich congenital muscular dystrophy in a consanguineous family: a case report

MLA

Pyara Rathnayake, et al. “A Novel Variant in the COL6A1 Gene Causing Ullrich Congenital Muscular Dystrophy in a Consanguineous Family: A Case Report.” BMC Neurology, vol. 21, Mar. 2021. EBSCOhost, https://doi.org/10.1186/s12883-021-02134-7.

APA

Pyara Rathnayake, A. Reghan Foley, C. Sampath Paththinige, Nirmala D. Sirisena, Vajira H. W. Dissanayake, B. A. P. Sajeewani Pathirana, Sandra Donkervoort, Carsten G. Bönnemann, U. M. Jayami Eshana Samaranayake, Osorio Abath Neto, & Nilaksha Neththikumara. (2021). A novel variant in the COL6A1 gene causing Ullrich congenital muscular dystrophy in a consanguineous family: a case report. BMC Neurology, 21. https://doi.org/10.1186/s12883-021-02134-7

Chicago

Pyara Rathnayake, A. Reghan Foley, C. Sampath Paththinige, Nirmala D. Sirisena, Vajira H. W. Dissanayake, B. A. P. Sajeewani Pathirana, Sandra Donkervoort, et al. 2021. “A Novel Variant in the COL6A1 Gene Causing Ullrich Congenital Muscular Dystrophy in a Consanguineous Family: A Case Report.” BMC Neurology 21 (March). doi:10.1186/s12883-021-02134-7.