Prevalence and founder effect of DRC1 exon 1–4 deletion in Korean patients with primary ciliary dyskinesia

MJ Kim, S Kim, SW Chae, S Lee, JG Yoon… - Journal of Human …, 2023 - nature.com
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder affecting ciliary
structure and function. PCD exhibiting dynein regulatory complex subunit 1 (DRC1) exon 1 …
被引用次数：7 相关文章

Prevalence and founder effect of DRC1 exon 1-4 deletion in Korean patients with primary ciliary dyskinesia

MJ Kim, S Kim, SW Chae, S Lee… - Journal of human …, 2023 - pubmed.ncbi.nlm.nih.gov
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder affecting ciliary
structure and function. PCD exhibiting dynein regulatory complex subunit 1 (DRC1) exon 1 …

Prevalence and founder effect of DRC1 exon 1-4 deletion in Korean patients with primary ciliary dyskinesia.

MJ Kim, S Kim, SW Chae, S Lee, JG Yoon… - Journal of Human …, 2023 - europepmc.org
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder affecting ciliary
structure and function. PCD exhibiting dynein regulatory complex subunit 1 (DRC1) exon 1 …

Prevalence and founder effect of DRC1 exon 1–4 deletion in Korean patients with primary ciliary dyskinesia

MJ Kim, S Kim, SW Chae, S Lee… - Journal of Human …, 2023 - snucm.elsevierpure.com
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder affecting ciliary
structure and function. PCD exhibiting dynein regulatory complex subunit 1 (DRC1) exon 1 …

Prevalence and founder effect of DRC1 exon 1–4 deletion in Korean patients with primary ciliary dyskinesia

MJ Kim, S Kim, SW Chae, S Lee… - Journal of Human …, 2023 - search.proquest.com
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder affecting ciliary
structure and function. PCD exhibiting dynein regulatory complex subunit 1 (DRC1) exon 1 …