Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C
Matsumoto, Namiko, Ohta, Yasuyuki, Deguchi, Kentaro, Kishida, Masayuki, Sato, Kota, Shang, Jingwei, Takemoto, Mami, Hishikawa, Nozomi, Yamashita, Toru, Watanabe, Aki, Yokote, Koutaro, Takemoto, MinoruYear:
2019
Language:
english
Journal:
Internal Medicine
DOI:
10.2169/internalmedicine.1816-18
File:
PDF, 422 KB
english, 2019