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9. A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease. Pratt VM, Trofatter JA, Schinzel A, Dlouhy SR, Conneally PM, Hodes ME. Am J Med Genet; 1991 Jan; 38(1):136-9. PubMed ID: 1707231 [Abstract] [Full Text] [Related]
10. An AG----GG transition at a splice site in the myelin proteolipid protein gene in jimpy mice results in the removal of an exon. Macklin WB, Gardinier MV, King KD, Kampf K. FEBS Lett; 1987 Nov 02; 223(2):417-21. PubMed ID: 2444462 [Abstract] [Full Text] [Related]
14. In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease. Kleindorfer DO, Dlouhy SR, Pratt VM, Jones MC, Trofatter JA, Hodes ME. Am J Med Genet; 1995 Feb 13; 55(4):405-7. PubMed ID: 7539213 [Abstract] [Full Text] [Related]
16. Lipophilin (PLP) gene in X-linked myelin disorders. Fahim S, Riordan JR. J Neurosci Res; 1986 Feb 13; 16(1):303-10. PubMed ID: 3746948 [Abstract] [Full Text] [Related]
17. Myelin proteolipid protein (PLP and DM-20) transcripts are deleted in jimpy mutant mice. Morello D, Dautigny A, Pham-Dinh D, Jollès P. EMBO J; 1986 Dec 20; 5(13):3489-93. PubMed ID: 2435545 [Abstract] [Full Text] [Related]
20. Girl with signs of Pelizaeus-Merzbacher disease heterozygous for a mutation in exon 2 of the proteolipid protein gene. Hodes ME, DeMyer WE, Pratt VM, Edwards MK, Dlouhy SR. Am J Med Genet; 1995 Feb 13; 55(4):397-401. PubMed ID: 7539211 [Abstract] [Full Text] [Related] Page: [Next] [New Search]