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Items: 4

1.
A Locus for Hereditary Sensory Neuropathy with Cough and Gastroesophageal Reflux on Chromosome 3p22-p24
C. Kok, M. L. Kennerson, P. J. Spring, A. J. Ing, J. D. Pollard, G. A. Nicholson
Am J Hum Genet. 2003 Sep; 73(3): 632–637. Published online 2003 Jul 17. doi: 10.1086/377591
PMCID:
PMC1180687
ArticlePubReaderPDF–148KCite
2.
Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.
E Nelis, V Timmerman, P De Jonghe, L Muylle, J J Martin, C Van Broeckhoven
J Med Genet. 1994 Oct; 31(10): 811–815. doi: 10.1136/jmg.31.10.811
PMCID:
PMC1050130
SummaryPage BrowsePDF–911KCite
3.
Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
Annachiara De Sandre-Giovannoli, Malika Chaouch, Serguei Kozlov, Jean-Michel Vallat, Meriem Tazir, Nadia Kassouri, Pierre Szepetowski, Tarik Hammadouche, Antoon Vandenberghe, Colin L. Stewart, Djamel Grid, Nicolas Lévy
Am J Hum Genet. 2002 Mar; 70(3): 726–736. Published online 2002 Jan 17. doi: 10.1086/339274
Correction in:
Am J Hum Genet. 2002 Apr; 70(4): 1075.
PMCID:
PMC384949
ArticlePubReaderPDF–687KCite
4.
Tracing Myelin Protein Zero (P0) in vivo by construction of P0-GFP fusion proteins
Arif B Ekici, Sevinc Oezbey, Christina Fuchs, Eva Nelis, Christine Van Broeckhoven, Melitta Schachner, Bernd Rautenstrauss
BMC Cell Biol. 2002; 3: 29. Published online 2002 Nov 26. doi: 10.1186/1471-2121-3-29
PMCID:
PMC139994
ArticlePubReaderPDF–1.7MCite

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