A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene - Concepedia

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A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

324

Citations

25

References

2000

Year

Maria Bitner‐Glindzicz, Keith Lindley, Paul Rutland, Diana C. Blaydon, Virpi V. Smith, Peter J. Milla, Khalid Hussain, Judith Furth-Lavi, Karen E. Cosgrove, Ruth M. Shepherd,

Nature Genetics

Infantile HyperinsulinismMendelian DisorderGenetic DisorderGeneticsClinical GeneticsPathologyUsher Type 1CMolecular GeneticsDisease Gene IdentificationDeafness IdentifiesMedicineMonogenic Disorders

References

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