Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2004-5-25
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1526-632X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
25
pubmed:volume
62
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1905-6
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:15159512-Adult, pubmed-meshheading:15159512-Amino Acid Substitution, pubmed-meshheading:15159512-Axons, pubmed-meshheading:15159512-Codon, pubmed-meshheading:15159512-Cough, pubmed-meshheading:15159512-Erectile Dysfunction, pubmed-meshheading:15159512-Female, pubmed-meshheading:15159512-Hereditary Sensory and Motor Neuropathy, pubmed-meshheading:15159512-Humans, pubmed-meshheading:15159512-Irritable Bowel Syndrome, pubmed-meshheading:15159512-Male, pubmed-meshheading:15159512-Mutation, Missense, pubmed-meshheading:15159512-Myelin P0 Protein, pubmed-meshheading:15159512-Pedigree, pubmed-meshheading:15159512-Point Mutation, pubmed-meshheading:15159512-Protein Structure, Tertiary, pubmed-meshheading:15159512-Reflex, Abnormal, pubmed-meshheading:15159512-Tonic Pupil, pubmed-meshheading:15159512-Urinary Incontinence
pubmed:year
2004
pubmed:articleTitle
Chronic cough due to Thr124Met mutation in the peripheral myelin protein zero (MPZ gene).
pubmed:affiliation
Department of Neurology, Massachusetts General Hospital, Boston, MA 02114, USA. rbaloh@partners.org
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports