Associated Papers
Prenatal diagnosis of rare genetic disorders: fourteen years' experience of a tertiary genetic centre from India.
Sheth J et al.
Orphanet Journal of Rare Diseases, 2025
40898337 (PubMed )
Supplement: 13023_2025_4003_MOESM4_ESM.xlsx › Other_rare_groups
Carnitine-acylcarnitine translocase deficiency: a case report with autopsy.
Thunga C et al.
Autopsy & Case Reports, 2024
Regulation of yeast actin behavior by interaction of charged residues across the interdomain cleft.
Yao X et al.
The Journal of Biological Chemistry, 2002
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