Cargando…
Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders
MED27 is a subunit of the Mediator multiprotein complex, which is involved in transcriptional regulation. Biallelic MED27 variants have recently been suggested to be responsible for an autosomal recessive neurodevelopmental disorder with spasticity, cataracts and cerebellar hypoplasia. We further de...
Ejemplares similares
-
Pitfalls in the diagnosis of Gaucher disease in Iraq: A diagnostic experience from a developing country
por: Thejeal, Rabab Farhan, et al.
Publicado: (2021) -
A Novel Homozygous ADCY5 Variant is Associated with a Neurodevelopmental Disorder and Movement Abnormalities
por: Kaiyrzhanov, Rauan, et al.
Publicado: (2021) -
Medication risk communication with cancer patients in a Middle East cancer care setting
por: Wilbur, Kerry, et al.
Publicado: (2016) -
Risk communication with Arab patients with cancer: a qualitative study of nurses and pharmacists
por: Wilbur, Kerry, et al.
Publicado: (2015) -
Genitourinary Symptoms Associated with Chlamydia trachomatis and Neisseria gonorrhoeae Infections in a Tertiary Care Hospital in Oman
por: Al-Muharrmi, Zakariya, et al.
Publicado: (2022)