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Heterozygous Ile453Val codon mutation in exon 7, homozygous single nucleotide polymorphisms in intron 2 and 5 of cathepsin C are associated with Haim-Munk syndrome

Identifieur interne : 000E84 ( Ncbi/Checkpoint ); précédent : 000E83; suivant : 000E85

Heterozygous Ile453Val codon mutation in exon 7, homozygous single nucleotide polymorphisms in intron 2 and 5 of cathepsin C are associated with Haim-Munk syndrome

Auteurs : Nalini Aswath [Inde] ; Bhuminathan Swamikannu [Inde] ; Sankar Narayanan Ramakrishnan [Inde] ; Rajendran Shanmugam [Inde] ; Jayakar Thomas [Inde] ; Arvind Ramanathan [Inde]

Source :

RBID : PMC:4054037

Abstract

Objective:

In the present study, we have investigated the genetic status of CTSC gene in a HMS subject, who along with her parents belonged to non-Jewish South Indian Dravidian community.

Materials and Methods:

Genomic deoxyribonucleic acid isolated from the peripheral blood of the subject was amplified with CTSC exon specific primers and were analyzed by direct sequencing.

Results:

Sequencing analysis identified Ile453Val mutation within exon 7 of CTSC gene in heterozygous condition, and two single nucleotide polymorphisms (SNPs) within intron 2 and 5 in homozygous condition.

Conclusion:

The present study has identified for the first time the association of Ile453Val mutation within exon 7 and the two SNPs in a subject with HMS.


Url:
DOI: 10.4103/1305-7456.126250
PubMed: 24966751
PubMed Central: 4054037


Affiliations:


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PMC:4054037

Le document en format XML

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<title>Objective:</title>
<p>In the present study, we have investigated the genetic status of
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gene in a HMS subject, who along with her parents belonged to non-Jewish South Indian Dravidian community.</p>
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<title>Materials and Methods:</title>
<p>Genomic deoxyribonucleic acid isolated from the peripheral blood of the subject was amplified with
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<sec id="st3">
<title>Results:</title>
<p>Sequencing analysis identified Ile453Val mutation within exon 7 of
<italic>CTSC</italic>
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<sec id="st4">
<title>Conclusion:</title>
<p>The present study has identified for the first time the association of Ile453Val mutation within exon 7 and the two SNPs in a subject with HMS.</p>
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<name sortKey="Ramakrishnan, Sankar Narayanan" sort="Ramakrishnan, Sankar Narayanan" uniqKey="Ramakrishnan S" first="Sankar Narayanan" last="Ramakrishnan">Sankar Narayanan Ramakrishnan</name>
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