A novel aminoterminal mutation in the KAL-1 gene in a large pedigree with X-linked Kallmann syndrome

Keyphrases

• X-linked 100%
• Large Pedigree 100%
• Kallmann Syndrome 100%
• Autosomal Recessive 20%
• Amino Acids 20%
• Autosomal Dominant 20%
• Clinical Features 20%
• Neurologic 20%
• Duplication 20%
• Hypogonadotropic Hypogonadism 20%
• Codon 20%
• Cell Adhesion Proteins 20%
• Three-mode 20%
• Frameshift 20%
• Mode of Inheritance 20%
• Direct Sequencing 20%
• Pedigree 20%
• Anosmia 20%
• Exon 1 20%

Biochemistry, Genetics and Molecular Biology

• Pedigree 100%
• Amino Acids 33%
• Exon 33%
• Autosomal Dominant Inheritance 33%
• Autosomal Recessive Inheritance 33%
• Cell Adhesion Proteins 33%
• Codon 33%