Official title and information are available only for Plus and Premium subscribers.
Patent Pending All mutations resulting in the Juvenile variant of NCL have been shown to occur at the CLN3 gene on 16p12;[28] of the mutations known to cause JNCL, 85% result from a 1.02 kb deletion, with a loss of amino acids 154–438, while the remaining 15% appear to result from either point or frameshift mutations.
To see the additional information details please login and subscribe to a Plus or Premium account.
