A rare ANOS1 variant in siblings with Kallmann syndrome identified by whole exome sequencing

Author:

Lopategui D. M.1ORCID,Griswold A. J.2,Arora H.3,Clavijo R. I.3,Tekin M.2,Ramasamy R.3

Affiliation:

1. Clinical and Translational Science Institute; University of Miami; Miami FL USA

2. John P Hussman Institute for Human Genomics; University of Miami; Miami FL USA

3. Department of Urology; University of Miami; Miami FL USA

Publisher

Wiley

Subject

Urology,Endocrinology,Reproductive Medicine,Endocrinology, Diabetes and Metabolism

Reference30 articles.

1. A global reference for human genetic variation;Auton;Nature,2015

2. The adhesion molecule anosmin-1 in neurology: Kallmann syndrome and beyond;Castro;Adv Neurobiol,2014

3. ANOS1: a unified nomenclature for Kallmann syndrome 1 gene (KAL1) and anosmin-1;Castro;Brief Funct Genomics,2016

4. Whole-exome enrichment with the agilent SureSelect human all exon platform;Chen;Cold Spring Harb Protoc,2015

5. An overview of the MAGE gene family with the identification of all human members of the family;Chomez;Cancer Res,2001

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