Literature DB >> 20960655

Gene symbol: TPP1. Disease: Neuronal Ceroid Lipofuscinosis, late infantile.

Romina Kohan1, Vivien J Muller, Michael J Fietz, Adriana I Cismondi, Ana M Oller Ramírez, Inés Noher Halac.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2008        PMID： 20960655

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   5.881


× No keyword cloud information.
  1 in total

1.  Mutation update: Review of TPP1 gene variants associated with neuronal ceroid lipofuscinosis CLN2 disease.

Authors:  Emily Gardner; Mitch Bailey; Angela Schulz; Mikel Aristorena; Nicole Miller; Sara E Mole
Journal:  Hum Mutat       Date:  2019-07-26       Impact factor: 4.878
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.