Author:
Goizet Cyril,Coupry Isabelle,Rooryck Caroline,Taine Laurence,Dormoy Virginie,Lacombe Didier,Arveiler Benoît
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference9 articles.
1. Berger J, Moser HW, Forss-Petter S : Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment. Curr Opin Neurol 2001; 14: 305–312.
2. Schiffmann R, Boespflug-Tanguy O : An update on the leukodsytrophies. Curr Opin Neurol 2001; 14: 789–794.
3. Coupry I, Taine L, Goizet C et al: Leukodystrophy and oculocutaneous albinism in a child with an 11q14 deletion. J Med Genet 2001; 38: 35–39.
4. Jager D, Stockert E, Jager E et al: Serological cloning of a melanocyte rab guanosine 5-prime-triphosphate-binding protein and a chromosome condensation protein from a melanoma complementary DNA library. Cancer Res 2000; 60: 3584–3591.
5. Toomes C, James J, Wood AJ et al: Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis. Nat Genet 1999; 23: 421–424.
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