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CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT
Known as:
ADCADN
National Institutes of Health
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Related topics
Related topics
12 relations
Autosomal dominant inheritance
Cerebellar Ataxia
Cerebellar atrophy
DNMT1, ALA570VAL
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Review
2016
Review
2016
DIVM ot spot causes varied phenorypes of HSAN 1 with dementia and
C. Klein
,
MG Bird
,
+7 authors
G. Nicholson
2016
Corpus ID: 43441508
Background: Mutations in DNA methyltransferase 1(DNMI1)have been identified in 2 autosomal dominant syndromes: 1-) hereditary…
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