Facile discovery of red blood cell deformation and compromised membrane/skeleton assembly in Prader—Willi syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s11684-022-0962-x.pdf
Reference30 articles.
1. Baldini L, Robert A, Charpentier B, Labialle S. Phylogenetic and molecular analyses identify SNORD116 targets involved in the Prader—Willi syndrome. Mol Biol Evol 2022; 39(1): msab348
2. Butler MG, Miller JL, Forster JL. Prader—Willi syndrome—clinical genetics, diagnosis and treatment approaches: an update. Curr Pediatr Rev 2019; 15(4): 207–244
3. Ge MM, Gao YY, Wu BB, Yan K, Qin Q, Wang H, Zhou W, Yang L. Relationship between phenotype and genotype of 102 Chinese newborns with Prader—Willi syndrome. Mol Biol Rep 2019; 46(5): 4717–4724
4. Juriaans AF, Kerkhof GF, Hokken-Koelega ACS. The spectrum of the Prader—Willi-like pheno- and genotype: a review of the literature. Endocr Rev 2022; 43(1): 1–18
5. Tauber M, Hoybye C. Endocrine disorders in Prader—Willi syndrome: a model to understand and treat hypothalamic dysfunction. Lancet Diabetes Endocrinol 2021; 9(4): 235–246
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