Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1969-8-30
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-13716765, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-14000866, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-14007166, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-14220660, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-14328400, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-14467629, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-5235841, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-5243393, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-5317552, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-5904467, http://linkedlifedata.com/resource/pubmed/commentcorrection/5306139-6020474
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0002-9297
pubmed:author
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
275-84
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:5306139-Adenine Nucleotides, pubmed-meshheading:5306139-Adolescent, pubmed-meshheading:5306139-Adult, pubmed-meshheading:5306139-Aged, pubmed-meshheading:5306139-Child, pubmed-meshheading:5306139-Child, Preschool, pubmed-meshheading:5306139-Chromosome Aberrations, pubmed-meshheading:5306139-Chromosome Disorders, pubmed-meshheading:5306139-Color Vision Defects, pubmed-meshheading:5306139-Crossing Over, Genetic, pubmed-meshheading:5306139-Erythrocytes, pubmed-meshheading:5306139-Female, pubmed-meshheading:5306139-Glucosyltransferases, pubmed-meshheading:5306139-Glycogen Storage Disease, pubmed-meshheading:5306139-Heterozygote, pubmed-meshheading:5306139-Humans, pubmed-meshheading:5306139-Infant, pubmed-meshheading:5306139-Infant, Newborn, pubmed-meshheading:5306139-Leukocytes, pubmed-meshheading:5306139-Male, pubmed-meshheading:5306139-Metabolism, Inborn Errors, pubmed-meshheading:5306139-Methods, pubmed-meshheading:5306139-Middle Aged, pubmed-meshheading:5306139-Pedigree, pubmed-meshheading:5306139-Phosphorylase Kinase, pubmed-meshheading:5306139-Sex Chromosomes
pubmed:year
1969
pubmed:articleTitle
X-chromosomal inheritance of liver glycogenosis with phosphorylase kinase deficiency.
pubmed:publicationType
Journal Article