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Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.

Othmane KB, Johnson E, Menold M, Graham FL, Hamida MB, Hasegawa O, Rogala AD, Ohnishi A, Pericak-Vance M, Hentati F, Vance JM. Othmane KB, et al. Genomics. 1999 Dec 15;62(3):344-9. doi: 10.1006/geno.1999.6028. Genomics. 1999. PMID: 10644431

Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.

Othmane KB, Loeb D, Hayworth-Hodgte R, Hentati F, Rao N, Roses AD, Ben Hamida M, Pericak-Vance MA, Vance JM. Othmane KB, et al. Genomics. 1995 Jul 20;28(2):286-90. doi: 10.1006/geno.1995.1143. Genomics. 1995. PMID: 8530038

Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B.

Vance JM, Speer MC, Stajich JM, West S, Wolpert C, Gaskell P, Lennon F, Tim RM, Rozear M, Othmane KB, et al. Vance JM, et al. Among authors: othmane kb. Am J Hum Genet. 1996 Jul;59(1):258-62. Am J Hum Genet. 1996. PMID: 8659534 Free PMC article. No abstract available.

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.

McNally EM, Passos-Bueno MR, Bönnemann CG, Vainzof M, de Sá Moreira E, Lidov HG, Othmane KB, Denton PH, Vance JM, Zatz M, Kunkel LM. McNally EM, et al. Among authors: othmane kb. Am J Hum Genet. 1996 Nov;59(5):1040-7. Am J Hum Genet. 1996. PMID: 8900232 Free PMC article.

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