Publication | Open Access
Whole-exome sequencing identifies the first French MODY 6 family with a new mutation in the NEUROD1 gene
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Citations
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References
2020
Year
New MutationMendelian DisorderNeurogenomicsGenetic DisorderGeneticsWhole-exome Sequencing IdentifiesMolecular GeneticsNeuroscienceDisease Gene IdentificationNeurod1 GeneMedicineNeurogenetics
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