Pages
- SCN5A
- HEXA
- Tay-Sachs Disease- Symptoms, Life Expectancy, and Genetic Testing
- Lactose Intolerance: Causes, Symptoms, Solutions & Your Genetic Link
- Myocardial Infarction
- SCN1A
- DEPDC5
- BSND : barttin CLCNK type accessory subunit beta
- PPT1 : palmitoyl-protein thioesterase 1
- CLN3 : CLN3 lysosomal/endosomal transmembrane protein, battenin
- CLN6 : CLN6 transmembrane ER protein
- CTNS : cystinosin, lysosomal cystine transporter
- DNM1L
- FUCA1 : alpha-L-fucosidase 1
- CYP1B1 : cytochrome P450 family 1 subfamily B member 1
- SLC2A1 : solute carrier family 2 member 1
- PYGM : glycogen phosphorylase, muscle associated
- PEX1 : peroxisomal biogenesis factor 1
- PEX6
- NLRP7 : NLR family pyrin domain containing 7
Blogs
- 6 foods that Boost Your Brain
- Of Strokes, Migraines, Dementia: A Story of CADASIL
- Lifestyle Disorders: Cardiovascular Diseases
- Lifestyle Disorders: Atrial Fibrillation and Stroke
- Lifestyle Disorders: Venous Thromboembolism
- Knowing the risk of Myocardial Infarction (Heart Attack) through Genetic Screening