Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1991-8-2
pubmed:abstractText
mRNA from a postmortem liver sample of a patient with classical phenylketonuria was examined using the chemical cleavage of mismatch (CCM) method to search for mutations in phenylalanine hydroxylase. Initial screening identified a heterozygous alteration in exon 2 which changed the encoded amino acid from phenylalanine (TTC) to leucine (TTG) at codon 39 and a polymorphism at codon 430 where the change from CTG to CTC did not alter the encoded leucine. Use of the CCM technique also revealed that the control reference clone differed from the published sequence by having a substitution of isoleucine (ATT) for methionine (ATG) at codon 276 and CAA rather than CAG as the codon for glutamine 232. By using the mRNA from the patient instead of the control as the source for the radiolabeled probe for the CCM technique, a second previously undetected alteration was identified in exon 10 where the change from TCA to CCA at codon 349 altered the amino acid from serine to arginine. Judicious choice of probes gives the CCM method the potential to detect close to 100% of single base mutations.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-1671810, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-1692838, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-1967207, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-1990848, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2116088, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2315047, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2320432, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2378353, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2474822, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2483035, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2574153, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2643100, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-265521, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2690813, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2726481, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2787020, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2884570, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-291982, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2986678, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-2999980, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-3017615, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-3018584, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-3260032, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-3431465, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-3475690, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-3969155, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-4071043, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-496890, http://linkedlifedata.com/resource/pubmed/commentcorrection/2063869-6220406
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0002-9297
pubmed:author
pubmed:issnType
Print
pubmed:volume
49
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
175-83
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed:year
1991
pubmed:articleTitle
Mutation detection in phenylketonuria by using chemical cleavage of mismatch: importance of using probes from both normal and patient samples.
pubmed:affiliation
Olive Miller Protein Laboratory, Murdoch Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't