rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
46
|
pubmed:dateCreated |
2009-1-22
|
pubmed:abstractText |
To identify a better non-invasive method to detect the carrier of mitochondrial A3243G mutation, a cause of mitochondrial encephalopathy-lactic acidosis-stroke like episode (MELAS) syndrome.
|
pubmed:language |
chi
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0376-2491
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
16
|
pubmed:volume |
88
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
3250-3
|
pubmed:meshHeading |
pubmed-meshheading:19159547-Adolescent,
pubmed-meshheading:19159547-Adult,
pubmed-meshheading:19159547-Child,
pubmed-meshheading:19159547-Child, Preschool,
pubmed-meshheading:19159547-DNA, Mitochondrial,
pubmed-meshheading:19159547-DNA Mutational Analysis,
pubmed-meshheading:19159547-Female,
pubmed-meshheading:19159547-Humans,
pubmed-meshheading:19159547-Infant,
pubmed-meshheading:19159547-MELAS Syndrome,
pubmed-meshheading:19159547-Male,
pubmed-meshheading:19159547-Middle Aged,
pubmed-meshheading:19159547-Pedigree,
pubmed-meshheading:19159547-Polymerase Chain Reaction,
pubmed-meshheading:19159547-Polymorphism, Restriction Fragment Length
|
pubmed:year |
2008
|
pubmed:articleTitle |
[Identification of an ideal noninvasive method to detect A3243G gene mutation in MELAS syndrome].
|
pubmed:affiliation |
Department of Central Laboratory, Peking University First Hospital, Beijing 100034, China.
|
pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
|