Seventeen novelPLP1mutations in patients with Pelizaeus-Merzbacher disease-Reference-Cited by-同舟云学术

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Seventeen novelPLP1mutations in patients with Pelizaeus-Merzbacher disease

Published:2005-02-14 Issue:3 Volume:25 Page:321-322
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Hübner Christian A.,Orth Ulrike,Senning Arne,Steglich Cordula,Kohlschütter Alfried,Korinthenberg Rudolf,Gal Andreas

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 34 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Exploring SVA Insertion Polymorphisms in Shaping Differential Gene Expressions in the Central Nervous System;Biomolecules;2024-03-17

2. Dört Aileden Pelizaeus-Merzbacher Sendromlu Altı Hastanın Klinik ve Moleküler Sitogenetik Analizleri;Turkish Journal of Pediatric Disease;2023-07-11

3. Familial 5.29 Mb deletion in chromosome Xq22.1–q22.3 with a normal phenotype: a rare pedigree and literature review;BMC Medical Genomics;2023-05-22

4. Genotype–phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus–merzbacher disease;Orphanet Journal of Rare Diseases;2022-03-28

5. Oligodendrocyte: Structure, Function and Pathology;The Biology of Glial Cells: Recent Advances;2022

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