Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis Patients.

Alkhzouz, Camelia; Cabau, Georgiana; Lazea, Cecilia; Asavoaie, Carmen; Bucerzan, Simona; Mirea, Andreea Manuela; Farcas, Marius; Miclaus Jnr, Maria; Popp, Radu; Miclea, Diana

Alkhzouz, Camelia; Cabau, Georgiana; Lazea, Cecilia; Asavoaie, Carmen; Bucerzan, Simona; Mirea, Andreea Manuela; Farcas, Marius; Miclaus Jnr, Maria; Popp, Radu; Miclea, Diana.

Afiliación

Alkhzouz C; Department of Medical Genetics, Clinical Emergency Hospital for Children, Cluj-Napoca, Romania.
Cabau G; "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Lazea C; "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Asavoaie C; "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Bucerzan S; First Pediatric Clinic, Clinical Emergency Hospital for Children, Cluj-Napoca, Romania.
Mirea AM; First Pediatric Clinic, Clinical Emergency Hospital for Children, Cluj-Napoca, Romania.
Farcas M; Department of Medical Genetics, Clinical Emergency Hospital for Children, Cluj-Napoca, Romania.
Miclaus Jnr M; "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Popp R; "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Miclea D; "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Pharmgenomics Pers Med ; 14: 349-358, 2021.

Article en En | MEDLINE | ID: mdl-33889011

Palabras clave

ApaI; BsmI; FokI; TaqI; mucopolysaccharidosis; vitamin D receptor

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pharmgenomics Pers Med Año: 2021 Tipo del documento: Article País de afiliación: Rumanía Pais de publicación: Nueva Zelanda

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