Associated Papers
Analysis of clinical and genetic features in an adolescent patient with primary ciliary dyskinesia induced by homozygous mutation in the RSPH4A gene: a case report.
Xu W et al.
Frontiers in Pediatrics, 2025
A novel homozygous RSPH4A variant in a family with primary ciliary dyskinesia and literature review.
Shen C et al.
Frontiers in Genetics, 2024
The RSPH4A Gene in Primary Ciliary Dyskinesia.
De Jesús-Rojas W et al.
International Journal of Molecular Sciences, 2023
Clinical and genetic features of primary ciliary dyskinesia in a cohort of consecutive clinically suspect children in western China.
Li Y et al.
Bmc Pediatrics, 2022
Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia-Related Infertility in Three Chinese Families.
Wang L et al.
Frontiers in Genetics, 2022
A Fetus with Ciliopathy Caused by a RSPH4A Variant Diagnosed Due to Increased Ventricular Size.
Zhen L et al.
Journal of Medical Ultrasound, 0
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