Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-3-12
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0148-7299
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
99
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
161-3
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11241479-Aminopeptidases, pubmed-meshheading:11241479-Asian Continental Ancestry Group, pubmed-meshheading:11241479-Base Sequence, pubmed-meshheading:11241479-Child, Preschool, pubmed-meshheading:11241479-DNA, pubmed-meshheading:11241479-DNA Mutational Analysis, pubmed-meshheading:11241479-Dipeptidyl-Peptidases and Tripeptidyl-Peptidases, pubmed-meshheading:11241479-Endopeptidases, pubmed-meshheading:11241479-Exons, pubmed-meshheading:11241479-Humans, pubmed-meshheading:11241479-Male, pubmed-meshheading:11241479-Molecular Sequence Data, pubmed-meshheading:11241479-Mutation, pubmed-meshheading:11241479-Neuronal Ceroid-Lipofuscinoses, pubmed-meshheading:11241479-Peptide Hydrolases, pubmed-meshheading:11241479-Sequence Analysis, DNA, pubmed-meshheading:11241479-Serine Proteases
pubmed:year
2001
pubmed:articleTitle
Two novel CLN2 gene mutations in a Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis.
pubmed:publicationType
Letter, Case Reports