Difference between revisions of "Ortiz-Gonzales X"
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{{Person}} | {{Person | ||
{{Labelingperson}} | |lastname=Ortiz-Gonzales | ||
|firstname=Xilma | |||
|institution=Center for Mitochondrial and Epigenomic Medicine (CMEM) | |||
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The Children's Hospital of Philadelphia - Research Institute | |||
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Colket Translational Research Building | |||
|address=3501 Civic Center Blvd | |||
|area code=19104 | |||
|city=Philadelphia | |||
|state=Pennsylvania (PA) | |||
|country=USA | |||
}} | |||
{{Labelingperson | |||
|field of research=Basic | |||
}} | |||
== O2k-Workshop == | |||
* [[MiPNet19.06 IOC 2014-06 Philadelphia | IOC91 Philadelphia]] |
Revision as of 14:18, 29 May 2014
Name | Ortiz-Gonzales Xilma, |
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Institution | Center for Mitochondrial and Epigenomic Medicine (CMEM)
The Children's Hospital of Philadelphia - Research Institute Colket Translational Research Building |
Address | 3501 Civic Center Blvd, 19104 |
City | Philadelphia |
State/Province | Pennsylvania (PA) |
Country | USA |
[email protected] | |
Weblink | |
O2k-Network Lab | US PA Philadelphia Wallace DC |
Labels:
Field of research: Basic
Publications
Published | Reference | |
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Gustafson 2019 PLoS One | 2019 | Gustafson MA, McCormick EM, Perera L, Longley MJ, Bai R, Kong J, Dulik M, Shen L, Goldstein AC, McCormack SE, Laskin BL, Leroy BP, Ortiz-Gonzalez XR, Ellington MG, Copeland WC, Falk MJ (2019) Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromes. PLoS One 14:e0221829. |