A Novel Aminoterminal Mutation in the KAL-1 Gene in a Large Pedigree with X-Linked Kallmann Syndrome
- 30 September 1998
- journal article
- case report
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 65 (1) , 59-61
- https://doi.org/10.1006/mgme.1998.2732
Abstract
No abstract availableKeywords
This publication has 1 reference indexed in Scilit:
- A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3)Nucleic Acids Research, 1991