CNKSR2 gene mutation leads to Houge type of X-linked syndromic mental retardation
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DOI: 10.1097/md.0000000000026093
Abstract: Abstract Rationale: Mutations of connector enhancer of kinase suppressor of Ras-2 (CNKSR2) gene were identified as the cause of Houge type of X-linked syndromic mental retardation. The mutations of CNKSR2 gene are rare, we reporta… read more here.
Keywords: syndromic mental; linked syndromic; cnksr2 gene; gene ... See more keywords