10490142

Source:http://linkedlifedata.com/resource/pubmed/id/10490142

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001898, umls-concept:C0019046, umls-concept:C0205419, umls-concept:C0369765, umls-concept:C0598629, umls-concept:C0871161, umls-concept:C0910659, umls-concept:C1706089
pubmed:issue	3
pubmed:dateCreated	1999-12-20
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7705865
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Alanine, http://linkedlifedata.com/resource/pubmed/chemical/Hemoglobins, Abnormal, http://linkedlifedata.com/resource/pubmed/chemical/Oxygen, http://linkedlifedata.com/resource/pubmed/chemical/Proline
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	0363-0269
pubmed:author	pubmed-author:GalactérosFF, pubmed-author:KisterJJ, pubmed-author:ProméDD, pubmed-author:RiouJJ, pubmed-author:WajcmanHH
pubmed:issnType	Print
pubmed:volume	23
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	281-6
pubmed:dateRevised	2005-8-25
pubmed:meshHeading	pubmed-meshheading:10490142-Adult, pubmed-meshheading:10490142-Alanine, pubmed-meshheading:10490142-European Continental Ancestry Group, pubmed-meshheading:10490142-France, pubmed-meshheading:10490142-Hematologic Tests, pubmed-meshheading:10490142-Hemoglobins, Abnormal, pubmed-meshheading:10490142-Humans, pubmed-meshheading:10490142-Oxygen, pubmed-meshheading:10490142-Point Mutation, pubmed-meshheading:10490142-Polycythemia, pubmed-meshheading:10490142-Proline, pubmed-meshheading:10490142-Solubility
pubmed:year	1999
pubmed:articleTitle	Hb Brie Comte Robert [beta36(C2)Pro-->Ala]: a new hemoglobin variant with high oxygen affinity and marked hydrophobic properties.
pubmed:affiliation	INSERM U 468, Hôpital Henri Mondor, Créteil, France. wajcman@im3.inserm.fr
pubmed:publicationType	Journal Article, Case Reports