A family of Melnick-Needles syndrome: a case report
Abstract Background Melnick-Needles syndrome (MNS) is an extremely rare osteochondrodysplasia caused by a mutation of FLNA, the gene encoding filamin A. MNS is inherited in an X-linked dominant manner. In this study, we describe three members of the same family with MNS, who exhibited different phen...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
BMC,
2020-08-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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