Refined assignment of the infantile neuronal ceroid‐lipofuscinosis (INCL) locus at 1p32 and the current status of prenatal and carrier diagnostics
- 1 March 1993
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 16 (2) , 335-338
- https://doi.org/10.1007/bf00710277
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
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- DNA‐based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1)Prenatal Diagnosis, 1991
- Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villiPrenatal Diagnosis, 1990
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- Infantile type of so-called neuronal ceroid-lipofuscinosisJournal of the Neurological Sciences, 1973