Literature DB >> 34515336

Novel bi-allelic HPDL variants cause hereditary spastic paraplegia in a Chinese patient.

Hao Yu1, Qiao Wei1, Wen-Jiao Luo1, Zhi-Ying Wu1.   

Abstract

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Year:  2021        PMID： 34515336     DOI： 10.1111/cge.14056

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  1 in total

1.  Case Report: Two Families With HPDL Related Neurodegeneration.

Authors:  Ieva Micule; Baiba Lace; Nathan T Wright; Nicolas Chrestian; Jurgis Strautmanis; Mikus Diriks; Janis Stavusis; Dita Kidere; Elfa Kleina; Anna Zdanovica; Nataly Laflamme; Nadie Rioux; Samarth Thonta Setty; Sander Pajusalu; Arnaud Droit; Monkol Lek; Serge Rivest; Inna Inashkina
Journal:  Front Genet       Date:  2022-02-09       Impact factor: 4.599
  1 in total

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