Transcobalamin deficiency caused by compound heterozygosity for two novel mutations in theTCN2gene: a study of two affected siblings, their brother, and their parents

✍ Scribed by Nissen, Peter H.; Nordwall, Maria; Hoffmann-Lücke, Elke; Sorensen, Boe S.; Nexo, Ebba

• Book ID: 125356662
• Publisher: Springer
• Year: 2010
• Tongue: English
• Weight: 247 KB
• Volume: 33
• Category: Article
• ISSN: 0141-8955
• DOI: 10.1007/s10545-010-9145-z