Cita APA (7a ed.)

Alhamoudi, K. M., Barhoumi, T., Al-Eidi, H., Asiri, A., Nashabat, M., Alaamery, M., . . . Alfadhel, M. (2021). A homozygous nonsense mutation in DCBLD2 is a candidate cause of developmental delay, dysmorphic features and restrictive cardiomyopathy. Nature Portfolio.

Cita Chicago Style (17a ed.)

Alhamoudi, Kheloud M., et al. A Homozygous Nonsense Mutation in DCBLD2 Is a Candidate Cause of Developmental Delay, Dysmorphic Features and Restrictive Cardiomyopathy. Nature Portfolio, 2021.

Cita MLA (8a ed.)

Alhamoudi, Kheloud M., et al. A Homozygous Nonsense Mutation in DCBLD2 Is a Candidate Cause of Developmental Delay, Dysmorphic Features and Restrictive Cardiomyopathy. Nature Portfolio, 2021.