A maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient
Crossref DOI link: https://doi.org/10.1186/s13039-017-0324-6
Published Online: 2017-06-14
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Liang, Siying
Jiang, Nan
Li, Shuo
Jiang, Xiaohu
Yu, Dongyi