Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literature.

Hadipour, Fatemeh; Sarkheil, Peymaneh; Noruzinia, Mehrdad; Hadipour, Zahra; Baghdadi, Taghi; Shafeghati, Yousef

Hadipour, Fatemeh; Sarkheil, Peymaneh; Noruzinia, Mehrdad; Hadipour, Zahra; Baghdadi, Taghi; Shafeghati, Yousef.

Afiliação

Hadipour F; Department of Medical Genetics, Sarem Cell Research Center, Sarem Women Hospital, Tehran, Iran.

Indian J Hum Genet ; 19(1): 84-6, 2013 Jan.

Article em En | MEDLINE | ID: mdl-23901198

Palavras-chave

Fanconi-Bickel syndrome; Iranian novel mutation; glucose transporter 2gene; missed diagnosis of osteogenesis imperfecta

Texto completo

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722635
https://dx.doi.org/10.4103/0971-6866.112906

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3722635
https://dx.doi.org/10.4103/0971-6866.112906

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2013 Tipo de documento: Article