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VeloGene Articles & Resource
TurboMice™ - Rare Diseases Matter
Autoimmune Encephalitis (AE) is a rare neuro‑immune disorder characterised by central‑nervous‑system...
Biotinidase Deficiency (BTD) is an autosomal‑recessive inherited metabolic disorder. It is caused by...
IgG4-related disease (IgG4-RD) is a chronic progressive fibrosing inflammatory disorder that received...
What Is Congenital Thrombotic Thrombocytopenic Purpura?Congenital Thrombotic Thrombocytopenic Purpura...
What Is Isovaleric Acidemia?Isovaleric Acidemia (IVA) is a rare autosomal recessive inborn organic...
What Is Gangliosidosis?Gangliosidosis encompasses a group of autosomal recessive lysosomal storage...
What is CDKL5 Deficiency Disorder?CDKL5 Deficiency Disorder (CDD) is a rare X-linked genetic brain...
What Is Severe Congenital Neutropenia?Severe Congenital Neutropenia (SCN) is a rare inherited bone...
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