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Sian Lewis
Sian Lewis
University of Bristol
Genetics
Sibling
Human genome
Bioinformatics
Mutation
2
Papers
4
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0
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Reads (from PCD affected sibling) mapped to the human genome hg19 at the p.(G300D) mutation.
2015
PLOS ONE
A. Mesut Erzurumluoglu
Muslim M. Alsaadi
Santiago Rodriguez
Tahani S. Alotaibi
Philip A. I. Guthrie
Sian Lewis
Aasiya Ginwalla
Tom R. Gaunt
Khalid K. Alharbi
Fahad Alsaif
Basma M. Alsaadi
Ian N. M. Day
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Proxy Molecular Diagnosis from Whole-Exome Sequencing Reveals Papillon-Lefevre Syndrome Caused by a Missense Mutation in CTSC
2015
PLOS ONE
A. Mesut Erzurumluoglu
Muslim M. Alsaadi
Santiago Rodriguez
Tahani S. Alotaibi
Philip A. I. Guthrie
Sian Lewis
Aasiya Ginwalla
Tom R. Gaunt
Khalid K. Alharbi
Fahad Alsaif
Basma M. Alsaadi
Ian N. M. Day
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Citations (4)
1