rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
6
|
pubmed:dateCreated |
2010-12-14
|
pubmed:abstractText |
To investigate the characteristics of the phenylalanine hydroxylase (PAH) gene mutations in patients with phenylketonuria (PKU) in Henan province, China, in order for providing basic information for clinical genetic counseling and prenatal diagnosis.
|
pubmed:language |
chi
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
1003-9406
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
27
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
644-9
|
pubmed:meshHeading |
pubmed-meshheading:21154324-Asian Continental Ancestry Group,
pubmed-meshheading:21154324-Base Sequence,
pubmed-meshheading:21154324-Child,
pubmed-meshheading:21154324-Child, Preschool,
pubmed-meshheading:21154324-China,
pubmed-meshheading:21154324-DNA Mutational Analysis,
pubmed-meshheading:21154324-Female,
pubmed-meshheading:21154324-Genetic Counseling,
pubmed-meshheading:21154324-Humans,
pubmed-meshheading:21154324-Infant,
pubmed-meshheading:21154324-Male,
pubmed-meshheading:21154324-Molecular Sequence Data,
pubmed-meshheading:21154324-Mutation,
pubmed-meshheading:21154324-Phenylalanine Hydroxylase,
pubmed-meshheading:21154324-Phenylketonurias,
pubmed-meshheading:21154324-Prenatal Diagnosis
|
pubmed:year |
2010
|
pubmed:articleTitle |
[The mutation spectrum of phenylalanine hydroxylase gene in patients with phenylketonuria in Henan province].
|
pubmed:affiliation |
Genetic Laboratory, People and Family Planning Scientific Research Faculty in Henan Province, Zhengzhou, Henan, P.R. China. rainbowwfy@yahoo.com.cn
|
pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
|