The impact of CFNS-causing <it>EFNB1 </it>mutations on ephrin-B1 function
<p>Abstract</p> <p>Background</p> <p>Mutations of <it>EFNB1 </it>cause the X-linked malformation syndrome craniofrontonasal syndrome (CFNS). CFNS is characterized by an unusual phenotypic pattern of inheritance, because it affects heterozygous females more s...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
BMC,
2010-06-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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