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

Search Results

Filter
  • 1-1 of  1 results for ""DEVECİ, Kübra""
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

A Novel Double Homozygous BTD Gene Mutation in a Case of Profound Biotinidase Deficiency.

  • Source: Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi. may2023, Vol. 17 Issue 3, p250-252. 3p.

Record details

×
  • 1-1 of  1 results for ""DEVECİ, Kübra""