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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2009-4-13
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pubmed:abstractText |
Mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene can cause congenital bilateral absence of vas deferens. Yet, the spectrum and frequency of CFTR mutations in Indian males with congenital absence of vas deferens (CAVD) is unknown.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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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 |
1460-2350
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1229-36
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pubmed:meshHeading |
pubmed-meshheading:19181743-Amino Acid Sequence,
pubmed-meshheading:19181743-Cystic Fibrosis Transmembrane Conductance Regulator,
pubmed-meshheading:19181743-Gene Frequency,
pubmed-meshheading:19181743-Genotype,
pubmed-meshheading:19181743-Humans,
pubmed-meshheading:19181743-India,
pubmed-meshheading:19181743-Male,
pubmed-meshheading:19181743-Molecular Sequence Data,
pubmed-meshheading:19181743-Mutation,
pubmed-meshheading:19181743-Phenotype,
pubmed-meshheading:19181743-Sequence Alignment,
pubmed-meshheading:19181743-Urogenital Abnormalities,
pubmed-meshheading:19181743-Vas Deferens
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pubmed:year |
2009
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pubmed:articleTitle |
Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens.
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pubmed:affiliation |
Department of Biochemistry, Post Graduate Institute of Medical Education and Research, Chandigarh 160012, India.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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