HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia
10.1111/cge.12030
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2022
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sg-nus-scholar.10635-2353122024-04-17T08:36:32Z HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia Aminkeng, F MEDICINE Science & Technology Life Sciences & Biomedicine Genetics & Heredity 10.1111/cge.12030 CLINICAL GENETICS 83 1 31-32 2022-12-05T03:33:17Z 2022-12-05T03:33:17Z 2013-01-01 2022-11-30T19:45:06Z Editorial Aminkeng, F (2013-01-01). HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia. CLINICAL GENETICS 83 (1) : 31-32. ScholarBank@NUS Repository. https://doi.org/10.1111/cge.12030 0009-9163 1399-0004 https://scholarbank.nus.edu.sg/handle/10635/235312 en WILEY-BLACKWELL Elements |
| institution |
National University of Singapore |
| building |
NUS Library |
| continent |
Asia |
| country |
Singapore Singapore |
| content_provider |
NUS Library |
| collection |
ScholarBank@NUS |
| language |
English |
| topic |
Science & Technology Life Sciences & Biomedicine Genetics & Heredity |
| spellingShingle |
Science & Technology Life Sciences & Biomedicine Genetics & Heredity Aminkeng, F HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia |
| description |
10.1111/cge.12030 |
| author2 |
MEDICINE |
| author_facet |
MEDICINE Aminkeng, F |
| format |
Editorial |
| author |
Aminkeng, F |
| author_sort |
Aminkeng, F |
| title |
HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia |
| title_short |
HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia |
| title_full |
HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia |
| title_fullStr |
HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia |
| title_full_unstemmed |
HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia |
| title_sort |
hint1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia |
| publisher |
WILEY-BLACKWELL |
| publishDate |
2022 |
| url |
https://scholarbank.nus.edu.sg/handle/10635/235312 |
| _version_ |
1800915748854431744 |