VeloGene Articles & Resource

TurboMice™ - Rare Diseases Matter

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Congenital Thrombotic Thrombocytopenic(cTTP)
What Is Congenital Thrombotic Thrombocytopenic Purpura?Congenital Thrombotic Thrombocytopenic Purpura...
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Isovaleric Acidemia
What Is Isovaleric Acidemia?Isovaleric Acidemia (IVA) is a rare autosomal recessive inborn organic...
Gangliosidosis:GM1/GM2-Tay-Sachs/Sandhoff
What Is Gangliosidosis?Gangliosidosis encompasses a group of autosomal recessive lysosomal storage...
CDKL5 Deficiency Disorder (CDD)
What is CDKL5 Deficiency Disorder?CDKL5 Deficiency Disorder (CDD) is a rare X-linked genetic brain...
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Severe Congenital Neutropenia
What Is Severe Congenital Neutropenia?Severe Congenital Neutropenia (SCN) is a rare inherited bone...
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Familial Hypercholesterolemia
What Is Familial Hypercholesterolemia?Familial Hypercholesterolemia (FH) is the most common autosomal...
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Sickle Cell Disease
What Is Sickle Cell Disease?Sickle Cell Disease (SCD) is an autosomal recessive disorder characterized...
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Spinocerebellar Ataxia
What Is Spinocerebellar Ataxia?Spinocerebellar Ataxia (SCA) refers to a heterogeneous group of inherited...
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