Novel heterozygous mutation in TBX1 in an infant with hypocalcemic seizures

Patients with 22q11.2 deletion syndrome have characteristic facial appearance, palate abnormalities, hypoparathyroidism, thymic hypoplasia, and congenital heart disease. The 22q11.2 region includes TBX1 and 30 other genes. Analysis of Tbx1 transgenic mice showed that TBX1 was associated with the 22q...

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Detaylı Bibliyografya
Yayımlandı:Clin Pediatr Endocrinol
Asıl Yazarlar: Hasegawa, Kosei, Tanaka, Hiroyuki, Higuchi, Yousuke, Hayashi, Yumiko, Kobayashi, Katsuhiro, Tsukahara, Hirokazu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Japanese Society for Pediatric Endocrinology 2018
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6073064/
https://ncbi.nlm.nih.gov/pubmed/30083032
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.27.159
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