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Muggenthaler, Martina M. A.
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1

MNS1 variant associated with situs inversus and male infert..:

Leslie, Joseph S. ; Rawlins, Lettie E. ; Chioza, Barry A....
European Journal of Human Genetics.  28 (2019)  1 - p. 50-55 , 2019
Link: https://doi.org/10.1038/..
 
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2

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndr..:

Muggenthaler, Martina M. A. ; Chowdhury, Biswajit ; Hasan, S. Naimul...
PLOS Genetics.  13 (2017)  1 - p. e1006470 , 2017
Link: https://doi.org/10.1371/..
 
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3

MNS1 variant associated with situs inversus and male infert..:

Rawlins, Lettie E ; Fasham, James ; Muggenthaler, Martina M A..
http://dx.doi.org/10.1038/s41431-019-0489-z.  , 2020
Link: https://doi.org/10.1038/..
 
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4

MNS1 variant associated with situs inversus and male infert..:

Leslie, Joseph S ; Rawlins, Lettie E ; Chioza, Barry A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906318/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
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5

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndr..:

Muggenthaler, Martina M. A ; Chowdhury, Biswajit ; Hasan, S. Naimul...
http://dx.plos.org/10.1371/journal.pgen.1006470.  , 2017
Link: http://hdl.handle.net/10..
 
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6

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndr..:

Martina M A Muggenthaler ; Biswajit Chowdhury ; S Naimul Hasan...
http://europepmc.org/articles/PMC5230738?pdf=render.  , 2017
Link: https://doi.org/10.1371/..
 
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7

SCN5A Mutation Type and a Genetic Risk Score Associate Vari..:

Wijeyeratne, Yanushi ; Tanck, Michael ; Mizusawa, Yuka...
info:eu-repo/semantics/altIdentifier/doi/10.1161/CIRCGEN.120.002911.  , 2020
Link: https://hal.sorbonne-uni..
 
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8

SCN5A Mutation Type and a Genetic Risk Score Associate Vari..:

Wijeyeratne, Yanushi D ; Tanck, Michael W ; Mizusawa, Yuka...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7748043/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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9

SCN5A Mutation Type and a Genetic Risk Score Associate Vari..:

Wijeyeratne, Yanushi, D ; Tanck, Michael ; Mizusawa, Yuka...
info:eu-repo/semantics/altIdentifier/doi/10.1161/CIRCGEN.120.002911.  , 2020
Link: https://hal.sorbonne-uni..
 
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10

SCN5A Mutation Type and a Genetic Risk Score Associate Vari..:

Wijeyeratne, Yanushi, D ; Tanck, Michael ; Mizusawa, Yuka...
info:eu-repo/semantics/altIdentifier/doi/10.1161/CIRCGEN.120.002911.  , 2020
Link: https://hal.sorbonne-uni..
 
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11

SCN5A Mutation Type and a Genetic Risk Score Associate Vari..:

Wijeyeratne, Yanushi, D ; Tanck, Michael ; Mizusawa, Yuka...
info:eu-repo/semantics/altIdentifier/doi/10.1161/CIRCGEN.120.002911.  , 2020
Link: https://hal.sorbonne-uni..
 
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12

Hypomorphic PCNA mutation underlies a human DNA repair diso..:

Baple, Emma L ; Chambers, Helen ; Cross, Harold E...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC.  , 2014
Link: http://www.ncbi.nlm.nih...
 
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13

Supraventricular and ventricular arrhythmias: interventiona..:

Gopal, Razeen ; Muggenthaler, Martina ; Gall, Nicholas.
Medicine.  46 (2018)  10 - p. 640-645 , 2018
Link: https://doi.org/10.1016/..
 
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14

Electrophysiological investigation:

Muggenthaler, Martina ; Gopal, Razeen ; Schilling, Richard.
Medicine.  46 (2018)  8 - p. 458-463 , 2018
Link: https://doi.org/10.1016/..
 
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15

Hyaluronidase 2 deficiency is a molecular cause of cor tria..:

Chowdhury, Biswajit ; Xiang, Bo ; Muggenthaler, Martina..
International Journal of Cardiology.  209 (2016)  - p. 281-283 , 2016
Link: https://doi.org/10.1016/..
 
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