The identification of a novel splicing mutation in C1qB in a Japanese family with C1q deficiency: a case report.

Higuchi, Yousuke; Shimizu, Junya; Hatanaka, Michiyo; Kitano, Etsuko; Kitamura, Hajime; Takada, Hidetoshi; Ishimura, Masataka; Hara, Toshiro; Ohara, Osamu; Asagoe, Kenji; Kubo, Toshihide

Higuchi, Yousuke; Shimizu, Junya; Hatanaka, Michiyo; Kitano, Etsuko; Kitamura, Hajime; Takada, Hidetoshi; Ishimura, Masataka; Hara, Toshiro; Ohara, Osamu; Asagoe, Kenji; Kubo, Toshihide.

Afiliação

Shimizu J; Department of Pediatrics, National Hospital Organization Okayama Medical Center, 1711-1 Tamasu, Kita-ku, Okayama 701-1192, Japan. junshimi@okayama3.hosp.go.jp.

Pediatr Rheumatol Online J ; 11(1): 41, 2013 Oct 28.

Article em En | MEDLINE | ID: mdl-24160257

Texto completo

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874733
https://dx.doi.org/10.1186/1546-0096-11-41

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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/PMC3874733
https://dx.doi.org/10.1186/1546-0096-11-41

Imprimir

XML

PubMed Links

Buscar no Google

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