Variants in FREM1 and trisomy 18 identified in a neonatal progeria patient
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11033-023-08595-y.pdf
Reference19 articles.
1. Lessel D, Kubisch C (2019) Hereditary syndromes with signs of premature aging. Deutsches Ärzteblatt Int 116(29–30):489
2. Novelli G, Muchir A, Sangiuolo F, Helbling-Leclerc A, D’Apice MR, Massart C et al (2002) Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C. Am J Hum Genet 71(2):426–431
3. Arboleda G, Ramírez N, Arboleda H (2007) The neonatal progeroid syndrome (Wiedemann–Rautenstrauch): a model for the study of human aging? Exp Gerontol 42(10):939–943
4. Hou J-W (2009) Natural course of neonatal progeroid syndrome. Pediatr Neonatol 50(3):102–109
5. Sambrook J, Russell DW (2006) Purification of nucleic acids by extraction with phenol: chloroform. Cold Spring Harb Protoc 2006(1):pdb. prot4455
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