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September 1, 1999Human Molecular GeneticsOpen Access

A Molecular Analysis of the Yemenite Deaf-Blind Hypopigmentation Syndrome: SOX10 Dysfunction Causes Different Neurocristopathies

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Authors

NBNadège BondurandUniversité Paris CitéKKKirsten KuhlbrodtEvotec (Germany)VPVéronique PingaultHôpital Necker-Enfants Malades

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Bondurand et al. (1999) studied this question.

synapsesocial.com/papers/6a93a4feec4af56311ebbcf5https://doi.org/10.1093/hmg/8.9.1785
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  1. 1Functional Analysis of Sox10 Mutations Found in Human Waardenburg-Hirschsprung Patients1998 · 140 citations