A novel mutation in NPHS2 causing nephrotic syndrome in a Saudi Arabian family.

Al-Hamed, Mohamed; Sayer, John A; Al-Hassoun, Ibrahim; Aldahmesh, Mohamed A; Meyer, Brian

Al-Hamed, Mohamed; Sayer, John A; Al-Hassoun, Ibrahim; Aldahmesh, Mohamed A; Meyer, Brian.

Afiliação

Al-Hamed M; King Faisal Specialist Hospital and Research Centre , Department of Genetics, Riyadh , Saudi Arabia ; Institute of Human Genetics, International Centre of Life, Newcastle University , Central Parkway, Newcastle upon Tyne, NE1 3BZ UK.
Sayer JA; Institute of Human Genetics, International Centre of Life, Newcastle University , Central Parkway, Newcastle upon Tyne, NE1 3BZ UK.
Al-Hassoun I; King Faisal Specialist Hospital and Research Centre , Department of Genetics, Riyadh , Saudi Arabia.
Aldahmesh MA; King Faisal Specialist Hospital and Research Centre , Department of Genetics, Riyadh , Saudi Arabia.
Meyer B; King Faisal Specialist Hospital and Research Centre , Department of Genetics, Riyadh , Saudi Arabia.

NDT Plus ; 3(6): 545-8, 2010 Dec.

Article em En | MEDLINE | ID: mdl-25949463

Palavras-chave

NPHS2; homozygosity; nephrotic syndrome; podocin

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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: NDT Plus Ano de publicação: 2010 Tipo de documento: Article