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Joseph Z. Glustein

Shaare Zedek Medical Center

6

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107

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Lipoamide dehydrogenase deficiency in Ashkenazi Jews: An insertion mutation in the mitochondrial leader sequence

1997 Human Mutation
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Lipoamide dehydrogenase deficiency: A new cause for recurrent myoglobinuria

1997 Muscle & Nerve
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Anomalies of the nipple: an additional finding in CHARGE syndrome.

1996 American Journal of Medical Genetics
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TheMolecular BasisofCanavan(Aspartoacylase Deficiency) Disease inEuropeanNon-Jewish Patients

1995
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The molecular basis of Canavan (aspartoacylase deficiency) disease in European non-Jewish patients

1995 American Journal of Human Genetics
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Citations (51)