HMSNL in a 13-year-old Bulgarian girl

Author:

Baethmann Martina,Göhlich-Ratmann Gudrun,Schröder Johann M,Kalaydjieva Luba,Voit Thomas

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference11 articles.

1. Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24;Kalaydjieva;Nat Genet,1996

2. Dyck PJ, Chance P, Lebo R, Carney JA. Hereditary motor and sensory neuropathy. In: Dyck PJ, Thomas PK, editors. Peripheral neuropathy, third ed. Philadelphia, PA: WB Saunders, 1993:1094–1136.

3. Mitochondrial abnormalities in human sural nerves: fine structural evaluation of cases with mitochondrial myopathy, hereditary and nonhereditary neuropathies, and review of the literature;Schröder;Acta Neuropathol,1991

4. Infantile neuroaxonal dystrophy;Aicardi;Brain,1979

5. Généthon human linkage map;Gyapay;Nat Genet,1994

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