Tay-Sachs disease in Moroccan Jews: Deletion of a phenylalanine in the α-subunit of β-hexosaminidase

Keyphrases

• Ashkenazi Jews 50%
• Carrier Frequency 25%
• Codon 25%
• Enzyme Activity 25%
• Ethnic Groups 25%
• Hexosaminidase A 25%
• In-frame Deletion 25%
• Jewish 50%
• Jewish Family 25%
• Jewish Population 25%
• Lysosomal Storage Disease 25%
• Moroccan 75%
• Moroccan Jews 100%
• Moroccan Patients 25%
• Obligate Carrier 25%
• Phenylalanine 100%
• Subunit Assembly 25%
• Tay-Sachs 25%
• Tay-Sachs Disease 100%
• β-hexosaminidase 100%

Biochemistry, Genetics and Molecular Biology

• Allele 20%
• Codon 20%
• Enzyme Activity 20%
• Hexosaminidase 100%
• Messenger RNA 20%
• Obligate Carrier 20%
• Phenylalanine 100%
• Tay-Sachs Disease 100%

Pharmacology, Toxicology and Pharmaceutical Science

• Beta N Acetylhexosaminidase 100%
• Beta N Acetylhexosaminidase A 20%
• Epileptic Absence 20%
• Lysosome Storage Disease 20%
• Phenylalanine 100%
• Storage Disease 20%
• Tay Sachs Disease 100%