Genetic Dissection and Clinical Features of MODY6 (NEUROD1-MODY)
Genetic Dissection and Clinical Features of MODY6 (NEUROD1-MODY)
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Publisher
New York: Springer US
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Language
English
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Publisher
New York: Springer US
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Scope and Contents
Contents
Purpose of Review
MODY6 due to mutations in the gene NEUROD1 is very rare, and details on its clinical manifestation and pathogenesis are scarce. In this review, we have summarized all reported cases of MODY6 diagnosed by genetic testing, and examined their clinical features in detail.
Recent Findings
MODY6 is a low penetrant MODY, suggest...
Alternative Titles
Full title
Genetic Dissection and Clinical Features of MODY6 (NEUROD1-MODY)
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TN_cdi_proquest_miscellaneous_2185564952
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2185564952
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ISSN
1534-4827
E-ISSN
1539-0829
DOI
10.1007/s11892-019-1130-9
