80. A novel mutation in the HEX B gene causing infantile Sandhoff disease: A high throughput semi-automated method for genetic screening of newborns

Lehotay, Denis C.; Fitterer, Braden; Antonishyn, Nick A.; Gravel, Roy A.; Casey, Robin

doi:10.1016/j.ymgme.2009.10.097

Molecular Genetics and Metabolism

2010

DOI: 10.1016/j.ymgme.2009.10.097

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80. A novel mutation in the HEX B gene causing infantile Sandhoff disease: A high throughput semi-automated method for genetic screening of newborns

Denis C. Lehotay

Braden Fitterer

Nick A. Antonishyn

et al.

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80. A novel mutation in the HEX B gene causing infantile Sandhoff disease: A high throughput semi-automated method for genetic screening of newborns

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