Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia.
截断型 ARL6IP1 变异是导致致命性复杂性遗传性痉挛性截瘫的遗传原因
期刊:BMC Medical Genetics
影响因子:
doi:10.1186/s12881-019-0851-6
Wakil Salma M, Alhissi Safa, Al Dossari Haya, Alqahtani Ayesha, Shibin Sherin, Melaiki Brahim T, Finsterer Josef, Al-Hashem Amal, Bohlega Saeed, Alazami Anas M
