5 results for author:"Dincer P." in Literature citations
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| A dystroglycan mutation associated with limb-girdle muscular dystrophy. Hara Y., Balci-Hayta B., Yoshida-Moriguchi T., Kanagawa M., Beltran-Valero de Bernabe D., Gundesli H., Willer T., Satz J.S., Crawford R.W., Burden S.J. et al. N. Engl. J. Med. 364:939-946(2011) · UniProtKB (1) · Mapped (4) |
| Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy. Gundesli H., Talim B., Korkusuz P., Balci-Hayta B., Cirak S., Akarsu N.A., Topaloglu H., Dincer P. Am. J. Hum. Genet. 87:834-841(2010) · UniProtKB (1) · Mapped (3) |
| An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene. Balci B., Uyanik G., Dincer P., Gross C., Willer T., Talim B., Haliloglu G., Kale G., Hehr U., Winkler J. et al. Neuromuscul. Disord. 15:271-275(2005) · UniProtKB (1) · Mapped (8) |
| A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. Dincer P., Leturcq F., Richard I., Piccolo F., Yalnizoglu D., de Toma C., Akcoeren Z., Broux O., Deburgrave N., Brenguier L. et al. Ann. Neurol. 42:222-229(1997) · UniProtKB (1) |
| Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins. Richard I., Brenguier L., Dincer P., Roudaut C., Bady B., Burgunder J.-M., Chemaly R., Garcia C.A., Halaby G., Jackson C.E. et al. Am. J. Hum. Genet. 60:1128-1138(1997) · UniProtKB (1) · Mapped (3) |