v1
Niemann-Pick type B disease. Identification of a single codon deletion in the acid sphingomyelinase gene and genotype/phenotype correlations in type A and B patients.
Identifier:nobleid.org/w1/20260515/C7828BFA
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/C7828BFA)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims