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CORRECTION
Correction: BAG3-related myofibrillar myopathy: focus on its cardiac involvement
Feb 9, 2026
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por
Elise Daire
en
Articulos
,
CORRECTION
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Enfermedades Raras
,
Frontiers in Genetics
Correction: Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis
Ene 2, 2026
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por
Ting Xiong
en
Articulos
,
CORRECTION
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Enfermedades Raras
,
Frontiers in Genetics
Correction: MAPT mutation-induced behavioral variant frontotemporal dementia in an Asian patient: a multimodal biomarker case report resolving diagnostic challenges with Alzheimer’s disease
Dic 1, 2025
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por
Yan Zhang
en
Articulos
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CORRECTION
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Enfermedades Raras
,
Frontiers in Genetics
Correction: Individual and combined effects of the GSTM1, GSTT1, and GSTP1 polymorphisms on type 2 diabetes mellitus risk: a systematic review and meta-analysis
Dic 1, 2025
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por
Liang-shu Liu
en
Articulos
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CORRECTION
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Enfermedades Raras
,
Frontiers in Genetics
Correction: Validation of a genome-wide polygenic score for body mass index in South Asians
Nov 27, 2025
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por
Ramesh Menon
en
Articulos
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CORRECTION
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Enfermedades Raras
,
Frontiers in Genetics
Correction: A novel splicing variant in NBAS identified by minigene assay causes infantile liver failure syndrome type 2
Nov 7, 2025
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por
Anna Hu
en
Articulos
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CORRECTION
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Enfermedades Raras
,
Frontiers in Genetics
Correction to “Recent Statistical Innovations in Human Genetics”
Oct 30, 2025
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por
Wiley: Annals of Human Genetics: Table of Contents
en
Annals of Human Genetics
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Articulos
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CORRECTION
Annals of Human Genetics, EarlyView.