Juvenile Tay Sachs Disease Due to Compound Heterozygous Mutation in Hex-A Gene, with Early Sign of Bilateral Tremors
Ann Indian Acad Neurol
.
2022 May-Jun;25(3):502-505.
doi: 10.4103/aian.aian_577_21.
Epub 2022 Jan 5.
Authors
Jayesh Sheth
1
,
Ira Mohapatra
1
,
Gangotri Patra
1
,
Riddhi Bhavsar
1
,
Chandni Patel
1
,
Siddharth Shah
2
,
Aadhira Nair
1
Affiliations
1
Department of Biochemical and Molecular Genetics, FRIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad, India.
2
Consultant Pediatric Neurologist, Royal Institute of Child Neurosciences, Vastrapur, Ahmedabad, Gujarat, India.
PMID:
35936646
PMCID:
PMC9350779
DOI:
10.4103/aian.aian_577_21
No abstract available