7849723

Source:http://linkedlifedata.com/resource/pubmed/id/7849723

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0162309, umls-concept:C0332183, umls-concept:C0599155
pubmed:issue	10
pubmed:dateCreated	1995-3-16
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9208958
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/ABCD1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/ATP-Binding Cassette Transporters, http://linkedlifedata.com/resource/pubmed/chemical/Codon, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0964-6906
pubmed:author	pubmed-author:FuchsSS, pubmed-author:GasJJ, pubmed-author:MandelJ LJL, pubmed-author:SardeC OCO, pubmed-author:SchwingerEE, pubmed-author:WedemannHH
pubmed:issnType	Print
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1903-5
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:7849723-ATP-Binding Cassette Transporters, pubmed-meshheading:7849723-Adrenoleukodystrophy, pubmed-meshheading:7849723-Amino Acid Sequence, pubmed-meshheading:7849723-Base Sequence, pubmed-meshheading:7849723-Codon, pubmed-meshheading:7849723-Conserved Sequence, pubmed-meshheading:7849723-DNA Primers, pubmed-meshheading:7849723-Exons, pubmed-meshheading:7849723-Female, pubmed-meshheading:7849723-Humans, pubmed-meshheading:7849723-Male, pubmed-meshheading:7849723-Membrane Proteins, pubmed-meshheading:7849723-Molecular Sequence Data, pubmed-meshheading:7849723-Pedigree, pubmed-meshheading:7849723-Point Mutation, pubmed-meshheading:7849723-Polymerase Chain Reaction, pubmed-meshheading:7849723-Restriction Mapping, pubmed-meshheading:7849723-X Chromosome
pubmed:year	1994
pubmed:articleTitle	Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD).
pubmed:affiliation	Institut für Humagenetik, Medizinische Universität, Lübeck, Germany.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't