Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation

被引：0
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作者：
Christoph Welsch
Anna Katharina Flügel
Susanne Rondot
Egbert Schulze
Ishani Sircar
Judith Nußbaumer
Jörg Bojunga
机构：
[1] Goethe-University Hospital Frankfurt,Department of Internal Medicine 1
[2] MVZ Labor Dr. Limbach & Kollegen GbR,undefined
[3] endokrinologikum Frankfurt,undefined
来源：
BMC Endocrine Disorders | / 22卷
关键词：
Case report; MEN1; Truncating mutation; Frameshift; Clinical phenotype;
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