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Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR.
Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel.
The molecular basis of mucolipidosis type IV.
A physical and transcript map of the MCOLN1 gene region on human chromosome 19p13.3-p13.2.
Mapping of the mucolipidosis type IV gene to chromosome 19p and definition of founder haplotypes.
Chromosomes, Human, Pair 19
Chromosomes Human Pair 19