Cite
MLA Citation
Mathias Schwartz et al.. “How chromosomal deletions can unmask recessive mutations? Deletions in 10q11.2 associated with CHAT or SLC18A3 mutations lead to congenital myasthenic syndrome.” American journal of medical genetics, vol. 176, no. 1, 2018, pp. 151–155. http://access.bl.uk/ark:/81055/vdc_100056040209.0x00001d