Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

نتائج البحث

Filter
  • 1-10 ل  18 نتائج ل ""Development and Disorders of Fetal Brain""
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

Subjects: Exome sequencing; 0301 basic medicine; Heterozygote

  • Source: BMC NeurolBMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)BMC NeurologyBMC Neurology, BioMed Central, 2021, 21 (1), pp.78. ⟨10.1186/s12883-021-02113-y⟩

تفاصيل العنوان

×
  • 1-10 ل  18 نتائج ل ""Development and Disorders of Fetal Brain""