Autosomal recessive Alport syndrome caused by a novel COL4A4 splice site mutation: a case report

Detalles Bibliográficos
Autores principales: Šenjug, Petar, Nikuševa Martić, Tamara, Šenjug Perica, Marija, Oroz, Maja, Horaček, Matija, Ćuk, Martin, Abdović, Slaven, Galešić Ljubanović, Danica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Medical Schools 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852137/
https://www.ncbi.nlm.nih.gov/pubmed/31686460
http://dx.doi.org/10.3325/cmj.2019.60.458

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852137/
https://www.ncbi.nlm.nih.gov/pubmed/31686460
http://dx.doi.org/10.3325/cmj.2019.60.458

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