A recurrent homozygous NHLRC1 variant in siblings with Lafora disease

Nami Araya1, Yukitoshi Takahashi1, Masayuki Shimono2

  • 1National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders, NHO, Shizuoka, Japan.

Human Genome Variation
|August 8, 2018
PubMed

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