Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence (Q44910035)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence |
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Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence (English)
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Mantel I
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Brantley MA Jr
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Bellmann C
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Robson AG
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Holder GE
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Taylor A
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Anderson G
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Moore AT
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