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Sperm mitochondrial mutations as a cause of low sperm motility
Kumarasamy Thangaraj
,
Manjunath B. Joshi
, Alla G. Reddy
, Avinash A. Rasalkar
, Lalji Singh
*
*
Corresponding author for this work
Department of Ageing Research, Manipal School of Life Sciences, Manipal
Research output
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Contribution to journal
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Article
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peer-review
85
Citations (Scopus)
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INIS
adenosine triphosphate
20%
blood cells
20%
codons
20%
concentration
20%
cytochrome oxidase
60%
dna
40%
genes
40%
lysine
20%
men
20%
mitochondria
100%
mutations
100%
nucleotides
20%
ribonucleic acid
40%
serine
20%
sperm
100%
testing
20%
Biochemistry, Genetics and Molecular Biology
Adenosine Triphosphate
33%
Cytochrome C Oxidase
100%
Lysine
33%
Microsatellite DNA
33%
Missense
33%
Mitochondrial DNA
33%
Mitochondrial Gene
33%
Paternity Test
33%
Serine
33%
Silent Mutation
33%
Spermatozoon Motility
100%
Stop Codon
33%
Transfer RNA
66%