No abstract available
Keywords:
CTSA mutation; early infantile galactosialidosis; lysosomal storage disease; next-generation sequencing.
MeSH terms
-
Cathepsin A / genetics*
-
High-Throughput Nucleotide Sequencing / methods
-
Humans
-
Infant
-
Infant, Newborn
-
Lysosomal Storage Diseases / diagnosis
-
Lysosomal Storage Diseases / genetics*
-
Male
-
Mutation
Substances
-
CTSA protein, human
-
Cathepsin A
Supplementary concepts
-
Neuraminidase deficiency with beta-galactosidase deficiency