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January 1, 1993Human Molecular GeneticsOpen Access

A novel point mutation (D380A) and a rare deletion (1255deI55) in the glucocerebrosidase gene causing Gaucher's disease

Andrew J. Walley Ann Harris

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Abstract

Andrew J Walley, Ann Harris; A novel point mutation (D380A) and a rare deletion (1255deI55) in the glucocerebrosidase gene causing Gaucher's disease, Human Mole

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Cite This Study

Walley et al. (1993) studied this question.

synapsesocial.com/papers/6a723c7b31a3df82432a045c https://doi.org/10.1093/hmg/2.10.1737

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