A de novo or germline mutation in a family with Mucolipidosis III gamma: Implications for molecular diagnosis and genetic counseling

Mucolipidosis III (ML III) gamma is a very rare autosomal-recessive disorder characterized by the abnormal trafficking and subcellular localization of lysosomal enzymes due to mutations in the GNPTG gene. The present study consists of a report of a Brazilian compound heterozygote patient with ML III...

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Detalles Bibliográficos
Autores principales: Velho, Renata Voltolini, Alegra, Taciane, Sperb, Fernanda, Ludwig, Nataniel Floriano, Saraiva-Pereira, Maria Luiza, Matte, Ursula, Schwartz, Ida V.D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121289/
https://www.ncbi.nlm.nih.gov/pubmed/27896079
http://dx.doi.org/10.1016/j.ymgmr.2014.01.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121289/
https://www.ncbi.nlm.nih.gov/pubmed/27896079
http://dx.doi.org/10.1016/j.ymgmr.2014.01.002

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