Prenatal diagnosis of PLP1 duplication by single nucleotide polymorphism array in a family with Pelizaeus-Merzbacher disease-Reference-Cited by-同舟云学术

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Prenatal diagnosis of PLP1 duplication by single nucleotide polymorphism array in a family with Pelizaeus-Merzbacher disease

Published:2021-01-11 Issue:1 Volume:13 Page:1488-1497
ISSN:1945-4589
Container-title:Aging
language:en
Short-container-title:Aging

Author:

Xue Huili¹,Yu Aili²,Chen Xuemei¹,Lin Na¹,Lin Min¹,Huang Hailong¹,Xu Liangpu¹

Affiliation:

1. Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Gulou, Fuzhou 350001, Fujian Province, China

2. Reproductive Medicine Center, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Gulou, Fuzhou 350001, Fujian Province, China

Publisher

Impact Journals, LLC

Subject

Cell Biology,Aging

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1. Hereditary Spastic Paraplegia: An Update;International Journal of Molecular Sciences;2022-02-01

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