Cargando…
Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel
BACKGROUND: Inherited cystic kidney disorders are a common cause of end-stage renal disease. Over 50 ciliopathy genes, which encode proteins that influence the structure and function of the primary cilia, are implicated in cystic kidney disease. METHODS: To define the phenotype and genotype of cysti...
Autores principales: | Al-Hamed, Mohamed H, Kurdi, Wesam, Alsahan, Nada, Alabdullah, Zainab, Abudraz, Rania, Tulbah, Maha, Alnemer, Maha, Khan, Rubina, Al-Jurayb, Haya, Alahmed, Ahmed, Tahir, Asma I, Khalil, Dania, Edwards, Noel, Al Abdulaziz, Basma, Binhumaid, Faisal S, Majid, Salma, Faquih, Tariq, El-Kalioby, Mohamed, Abouelhoda, Mohamed, Altassan, Nada, Monies, Dorota, Meyer, Brian, Sayer, John A, Albaqumi, Mamdouh |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853542/ https://www.ncbi.nlm.nih.gov/pubmed/26862157 http://dx.doi.org/10.1136/jmedgenet-2015-103469 |
Ejemplares similares
-
Renal tubular dysgenesis: antenatal ultrasound scanning and molecular investigations in a Saudi Arabian family
por: Al-Hamed, Mohamed H., et al.
Publicado: (2016) -
Fetal Anomalies Associated with Novel Pathogenic Variants in TMEM94
por: Al-Hamed, Mohamed H., et al.
Publicado: (2020) -
Characterizing the morbid genome of ciliopathies
por: Shaheen, Ranad, et al.
Publicado: (2016) -
Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes
por: Roosing, Susanne, et al.
Publicado: (2016) -
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes
por: Waters, Aoife M, et al.
Publicado: (2015)