Diabetes in a Weiss-Kruszka Syndrome Boy and a De Novo Deletion in 9q31.2
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References
1.
Weiss K, Wigby K, Fannemel M, Henderson L, Beck N, Ghali N
. Haploinsufficiency of ZNF462 is associated with craniofacial anomalies, corpus callosum dysgenesis, ptosis, and developmental delay. Eur J Hum Genet. 2017; 25(8):946-951.
PMC: 5567153.
DOI: 10.1038/ejhg.2017.86.
View
2.
Wortmann S, Mayr J
. Choline-related-inherited metabolic diseases-A mini review. J Inherit Metab Dis. 2019; 42(2):237-242.
PMC: 7814885.
DOI: 10.1002/jimd.12011.
View
3.
Wang R, Guo S, Yang L
. Tal2 is required for generation of GABAergic neurons in the zebrafish midbrain. Dev Dyn. 2022; 252(2):263-275.
DOI: 10.1002/dvdy.534.
View
4.
Marini J, Blissett A
. New genes in bone development: what's new in osteogenesis imperfecta. J Clin Endocrinol Metab. 2013; 98(8):3095-103.
PMC: 3733862.
DOI: 10.1210/jc.2013-1505.
View
5.
Malick W, Schaefer E, Hegele R, Rosenson R
. ABCA1 Deficiency: A Rare Cause of Premature Coronary Artery Disease. JACC Case Rep. 2023; 18:101904.
PMC: 10401051.
DOI: 10.1016/j.jaccas.2023.101904.
View