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Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population.

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Title: Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population.
Authors: Cerón-Rodríguez M; Lysosomal Disorders Clinic, Hospital Infantil de México Federico Gómez, Mexico City, Mexico., Vázquez-Martínez ER; Unidad de Investigación en Reproducción Humana, Instituto Nacional de Perinatología-Facultad de Química, Universidad Nacional Autónoma de México, Mexico City, Mexico., García-Delgado C; Department of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico., Ortega-Vázquez A; Department of Biological Systems, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico., Valencia-Mayoral P; Department of Pathology, Hospital Infantil de México Federico Gómez, Mexico City, Mexico., Ramírez-Devars L; Lysosomal Disorders Clinic, Hospital Infantil de México Federico Gómez, Mexico City, Mexico., Arias-Villegas C; Department of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico., Monroy-Muñoz IE; Departamento de Genética y Genómica Humana, Instituto Nacional de Perinatología, Mexico City, Mexico., López M; Department of Biological Systems, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico., Cervantes A; Servicio de Genética, Hospital General de México Dr. Eduardo Liceaga-Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico., Cerbón M; Unidad de Investigación en Reproducción Humana, Instituto Nacional de Perinatología-Facultad de Química, Universidad Nacional Autónoma de México, Mexico City, Mexico., Morán-Barroso VF; Department of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico. Electronic address: veronicafmoranbarroso@comunidad.unam.mx.
Source: Annals of hepatology [Ann Hepatol] 2019 Jul - Aug; Vol. 18 (4), pp. 613-619. Date of Electronic Publication: 2019 May 12.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Fundación Clínica Médica Sur Country of Publication: Mexico NLM ID: 101155885 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1665-2681 (Print) Linking ISSN: 16652681 NLM ISO Abbreviation: Ann Hepatol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population.
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  Data: <searchLink fieldCode="AU" term="%22Cerón-Rodríguez+M%22">Cerón-Rodríguez M</searchLink>; Lysosomal Disorders Clinic, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Vázquez-Martínez+ER%22">Vázquez-Martínez ER</searchLink>; Unidad de Investigación en Reproducción Humana, Instituto Nacional de Perinatología-Facultad de Química, Universidad Nacional Autónoma de México, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22García-Delgado+C%22">García-Delgado C</searchLink>; Department of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Ortega-Vázquez+A%22">Ortega-Vázquez A</searchLink>; Department of Biological Systems, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Valencia-Mayoral+P%22">Valencia-Mayoral P</searchLink>; Department of Pathology, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Ramírez-Devars+L%22">Ramírez-Devars L</searchLink>; Lysosomal Disorders Clinic, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Arias-Villegas+C%22">Arias-Villegas C</searchLink>; Department of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Monroy-Muñoz+IE%22">Monroy-Muñoz IE</searchLink>; Departamento de Genética y Genómica Humana, Instituto Nacional de Perinatología, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22López+M%22">López M</searchLink>; Department of Biological Systems, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Cervantes+A%22">Cervantes A</searchLink>; Servicio de Genética, Hospital General de México Dr. Eduardo Liceaga-Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Cerbón+M%22">Cerbón M</searchLink>; Unidad de Investigación en Reproducción Humana, Instituto Nacional de Perinatología-Facultad de Química, Universidad Nacional Autónoma de México, Mexico City, Mexico.<br /><searchLink fieldCode="AU" term="%22Morán-Barroso+VF%22">Morán-Barroso VF</searchLink>; Department of Genetics, Hospital Infantil de México Federico Gómez, Mexico City, Mexico. Electronic address: veronicafmoranbarroso@comunidad.unam.mx.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Fundación+Clínica+Médica+Sur%22">Fundación Clínica Médica Sur </searchLink><i>Country of Publication: </i>Mexico <i>NLM ID: </i>101155885 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1665-2681 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2216652681%22">16652681 </searchLink><i>NLM ISO Abbreviation: </i>Ann Hepatol <i>Subsets: </i>MEDLINE
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