Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome (Q57632541)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome |
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Statements
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome (English)
Ana Paula Abreu
Ericka Barbosa Trarbach
Elaine Maria Frade Costa
Beatriz Versiani
Maria Tereza Matias Baptista
Heraldo Mendes Garmes
5 August 2008