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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
1999-6-3
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pubmed:abstractText |
The purpose of this study was to describe the clinical and molecular features of a large family with maternally inherited cardiomyopathy (MICM).
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0735-1097
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1584-9
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:10334428-Adolescent,
pubmed-meshheading:10334428-Adult,
pubmed-meshheading:10334428-Aged,
pubmed-meshheading:10334428-Aged, 80 and over,
pubmed-meshheading:10334428-Cardiomyopathy, Hypertrophic,
pubmed-meshheading:10334428-Child,
pubmed-meshheading:10334428-Child, Preschool,
pubmed-meshheading:10334428-DNA, Mitochondrial,
pubmed-meshheading:10334428-DNA Mutational Analysis,
pubmed-meshheading:10334428-Female,
pubmed-meshheading:10334428-Genetic Predisposition to Disease,
pubmed-meshheading:10334428-Heart Failure,
pubmed-meshheading:10334428-Humans,
pubmed-meshheading:10334428-Male,
pubmed-meshheading:10334428-Middle Aged,
pubmed-meshheading:10334428-Pedigree,
pubmed-meshheading:10334428-Phenotype,
pubmed-meshheading:10334428-Point Mutation,
pubmed-meshheading:10334428-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:10334428-Pregnancy,
pubmed-meshheading:10334428-RNA, Transfer, Ile,
pubmed-meshheading:10334428-Sex Chromosome Aberrations,
pubmed-meshheading:10334428-X Chromosome
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pubmed:year |
1999
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pubmed:articleTitle |
Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid.
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pubmed:affiliation |
Istituto di Clinica delle Malattie Nervose e Mentali, Università di Roma-La Sapienza, Rome, Italy. Casali@uniroma1.it
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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