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.

Afiliação

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 em En | MEDLINE | ID: mdl-33889011

Palavras-chave

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

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pharmgenomics Pers Med Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Romênia

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google