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@streetbeast21
Further research is dedicated to the G1706Ap.R569H mutation. A survey of previously reported cases established the mutation as the most prevalent mutation site within Kenny-Caffey syndrome type 2 (KCS2) cases observed to date, accounting for 16 out of 23 cases, or 69.6%. The mutation exhibited a slightly greater incidence in females compared to […] View
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Fitch Jackson posted an update a month ago
Further research is dedicated to the G1706Ap.R569H mutation. A survey of previously reported cases established the mutation as the most prevalent mutation site within Kenny-Caffey syndrome type 2 (KCS2) cases observed to date, accounting for 16 out of 23 cases, or 69.6%. The mutation exhibited a slightly greater incidence in females compared to…[Read more]
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Fitch Jackson became a registered member a month ago
