Cargando…
Adult GAMT deficiency: A literature review and report of two siblings
Guanidinoacetate methyltransferase (GAMT) deficiency is a creatine deficiency disorder and an inborn error of metabolism presenting with progressive intellectual and neurological deterioration. As most cases are identified and treated in early childhood, adult phenotypes that can help in understandi...
Autores principales: | Modi, Bhavi P., Khan, Haq Nawaz, van der Lee, Robin, Wasim, Muhammad, Haaxma, Charlotte A., Richmond, Phillip A., Drögemöller, Britt, Shah, Suleman, Salomons, Gajja, van der Kloet, Frans M., Vaz, Fred M., van der Crabben, Saskia N., Ross, Colin J., Wasserman, Wyeth W., van Karnebeek, Clara D.M., Awan, Fazli Rabbi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093930/ https://www.ncbi.nlm.nih.gov/pubmed/33996490 http://dx.doi.org/10.1016/j.ymgmr.2021.100761 |
Ejemplares similares
-
Dynamic software design for clinical exome and genome analyses: insights from bioinformaticians, clinical geneticists, and genetic counselors
por: Shyr, Casper, et al.
Publicado: (2016) -
A mild case of sodium-dependent multivitamin transporter (SMVT) deficiency illustrating the importance of treatment response in variant classification
por: Hauth, Ingeborg, et al.
Publicado: (2022) -
Biochemical Screening of Intellectually Disabled Patients: A Stepping Stone to Initiate a Newborn Screening Program in Pakistan
por: Wasim, Muhammad, et al.
Publicado: (2019) -
GeneBreaker: Variant simulation to improve the diagnosis of Mendelian rare genetic diseases
por: Richmond, Phillip A., et al.
Publicado: (2021) -
Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy
por: Modi, Bhavi P., et al.
Publicado: (2021)