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- W4200220132 abstract "To identify and characterize a novel deletion at the LHX4 gene locus in a proband with growth hormone deficiency (GHD). Long range polymerase chain reaction (PCR) amplification was used to confirm the suspected deletion and to identify the rough locations of the end points. Sanger sequencing was carried out to identify the exact end points of the deletion. Suspected deletion was confirmed via long range PCR amplification. Sanger sequencing identified the end points of the deletion within three nucleotide repeat sequences (“CTT”). The total length of the deleted segment was 12 127 base pairs and it includes complete exon 5 and exon 6 of the LHX4 gene. Therefore the homeodomain motif coded by exons 4 and 5, might be affected . We have identified a novel deletion that spans exon 5 and exon 6 of the LHX4 gene that could have occurred via microhomology mediated non-recurrent rearrangement. The deletion characterized does not appear to have been reported before. To our knowledge this novel deletion is the first identified LHX4 variant from Sri Lanka and it explains the phenotype of the proband characterized by growth hormone deficiency, hypoplastic anterior pituitary and subsequent deficiency of thyroid stimulating hormone and adrenocorticotropic hormone (ACTH). • Heterozygous deletions in LHX4 gene can develop pituitary hormone deficiencies. • Microhomology mediated genetic rearrangements cause heterozygous large deletions. • Deletions affecting the homeodomain motif cause loss of function of LHX4 protein. • Presence of non-functional LHX4 protein leads to pituitary defects." @default.
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- W4200220132 date "2021-12-01" @default.
- W4200220132 modified "2023-10-16" @default.
- W4200220132 title "Novel gross deletion at the LHX4 gene locus in achild with growth hormone deficiency" @default.
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- W4200220132 doi "https://doi.org/10.1016/j.ghir.2021.101443" @default.
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