{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T15:48:40Z","timestamp":1786636120353,"version":"build-2736575974"},"reference-count":45,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neurol India"],"published-print":{"date-parts":[[2010]]},"DOI":"10.4103\/0028-3886.72164","type":"journal-article","created":{"date-parts":[[2010,11,26]],"date-time":"2010-11-26T00:53:52Z","timestamp":1290732832000},"page":"691","source":"Crossref","is-referenced-by-count":10,"title":["Sarcoglycanopathy: Clinical and histochemical characteristics in 66 patients"],"prefix":"10.4103","volume":"58","author":[{"given":"A","family":"Nalini","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N","family":"Gayathri","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fazil","family":"Thaha","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sarala","family":"Das","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Shylashree","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"key-10.4103\/0028-3886.72164-1","first-page":"37","volume-title":"Psuedo-hypertrophic muscular paralysis","author":"Gowers","year":"1879","journal-title":"Lancet"},{"key":"key-10.4103\/0028-3886.72164-2","first-page":"353","volume-title":"Adhalin gene mutations and autosomal recessive limb-girdle muscular dystrophy","author":"Campbell","year":"1995","journal-title":"Ann Neurol"},{"key":"key-10.4103\/0028-3886.72164-3","first-page":"1711","volume-title":"Dystrophin associated proteins in muscular dystrophy","author":"Ozawa","year":"1995","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/0028-3886.72164-4","first-page":"195","volume-title":"Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene","author":"Nigro","year":"1996","journal-title":"Nat Genet"},{"key":"key-10.4103\/0028-3886.72164-5","first-page":"32321","volume-title":"Caracterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy","author":"Jung","year":"1996","journal-title":"J Biol Chem"},{"key":"key-10.4103\/0028-3886.72164-6","first-page":"320","volume-title":"Deficiency of the 50K-dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy","author":"Matsumura","year":"1992","journal-title":"Nature"},{"key":"key-10.4103\/0028-3886.72164-7","first-page":"469","volume-title":"Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia","author":"Ben","year":"1983","journal-title":"Muscle Nerve"},{"key":"key-10.4103\/0028-3886.72164-8","first-page":"799","volume-title":"Deficiency of the 50kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native in European countries","author":"Fardeau","year":"1993","journal-title":"C R Acad Sci III"},{"key":"key-10.4103\/0028-3886.72164-9","first-page":"70","volume-title":"Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency","author":"Romero","year":"1994","journal-title":"C R Acad Sci Paris III"},{"key":"key-10.4103\/0028-3886.72164-10","first-page":"196","volume-title":"Clinical heterogeneity of adhalin deficiency","author":"Morandi","year":"1996","journal-title":"Ann Neurol"},{"key":"key-10.4103\/0028-3886.72164-11","first-page":"1945","volume-title":"Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50-DAG analysis","author":"Passos-Bueno","year":"1993","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/0028-3886.72164-12","first-page":"1163","volume-title":"A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy","author":"Bueno","year":"1995","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/0028-3886.72164-13","first-page":"121","volume-title":"Deficiency of the 50kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two South Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy","author":"Sewry","year":"1994","journal-title":"Neuromuscul Discord"},{"key":"key-10.4103\/0028-3886.72164-14","first-page":"1202","volume-title":"Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency","author":"Kawai","year":"1995","journal-title":"J Clin Invest"},{"key":"key-10.4103\/0028-3886.72164-15","first-page":"551","volume-title":"The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: Immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin","author":"Hayashi","year":"1995","journal-title":"Neurology"},{"key":"key-10.4103\/0028-3886.72164-16","first-page":"1841","volume-title":"Mutations that disrupt the carboxyl terminus of a-sarcoglycan cause muscular dystrophy","author":"McNally","year":"1996","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/0028-3886.72164-17","first-page":"143","volume-title":"Biochemical identification of d-sarcoglycan","author":"Yoshida","year":"1997","journal-title":"FEBS Lett"},{"key":"key-10.4103\/0028-3886.72164-18","first-page":"748","volume-title":"Glycoprotein complex anchoring dystrophin to sarcolemma","author":"Yoshida","year":"1990","journal-title":"J Biochem"},{"key":"key-10.4103\/0028-3886.72164-19","first-page":"266","volume-title":"Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex","author":"Bonnemann","year":"1995","journal-title":"Nat Genet"},{"key":"key-10.4103\/0028-3886.72164-20","first-page":"257","volume-title":"Beta-sarcoglycan: Characterization and role in the limb-girdle dystrophy linked to 4q12","author":"Lim","year":"1995","journal-title":"Nat Genet"},{"key":"key-10.4103\/0028-3886.72164-21","first-page":"819","volume-title":"Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy","author":"Noguchi","year":"1995","journal-title":"Science"},{"key":"key-10.4103\/0028-3886.72164-22","first-page":"625","volume-title":"Missense mutations in adhalin gene linked to autosomal recessive muscular dystrophy","author":"Roberds","year":"1994","journal-title":"Cell"},{"key":"key-10.4103\/0028-3886.72164-23","first-page":"1227","volume-title":"Primary adhalinopathy (sarcoglycanopathy): Clinical, pathologic and genetic correlation in 20 patients with autosomal recessive muscular dystrophy","author":"Eymard","year":"1997","journal-title":"Neurology"},{"key":"key-10.4103\/0028-3886.72164-24","first-page":"973","volume-title":"Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations","author":"Fanin","year":"1997","journal-title":"J Med Genet"},{"key":"key-10.4103\/0028-3886.72164-25","first-page":"446","volume-title":"Sarcoglycanopathies: An enigmatic form of muscular dystrophy- A report of 7 cases","author":"Sharma","year":"2004","journal-title":"Neurol India","ISSN":"https:\/\/id.crossref.org\/issn\/0028-3886","issn-type":"print"},{"key":"key-10.4103\/0028-3886.72164-26","first-page":"27","volume-title":"Sarcoglycanopathies.A report of 25 cases","author":"Khadilkar","year":"2002","journal-title":"Neurol India","ISSN":"https:\/\/id.crossref.org\/issn\/0028-3886","issn-type":"print"},{"key":"key-10.4103\/0028-3886.72164-27","first-page":"117","volume-title":"Sarcoglycanopathies: A clinico-pathological study","author":"Meena","year":"2007","journal-title":"Neurol India","ISSN":"https:\/\/id.crossref.org\/issn\/0028-3886","issn-type":"print"},{"key":"key-10.4103\/0028-3886.72164-28","first-page":"584","volume-title":"Limb girdle muscular dystrophy.A pathological and immunohistochemical re-evaluation","author":"Van","year":"1998","journal-title":"Muscle Nerve"},{"key":"key-10.4103\/0028-3886.72164-29","first-page":"1735","volume-title":"Limb-girdle muscular dystrophy in Guipuzcoa (Basque Country, Spain)","author":"Urtasun","year":"1998","journal-title":"Brain"},{"key":"key-10.4103\/0028-3886.72164-30","first-page":"475","volume-title":"Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex","author":"Duggan","year":"1996","journal-title":"Neuromuscul Disord"},{"key":"key-10.4103\/0028-3886.72164-31","first-page":"463","volume-title":"From adhalinopathies to alpha-sarcoglycanopathies: An overview","author":"Jeanpierre","year":"1996","journal-title":"Neuromuscul Disord"},{"key":"key-10.4103\/0028-3886.72164-32","first-page":"28","volume-title":"Concomitant deficiency of b-and g-sarcoglycans in 20 a-sarcoglycan (adhalin)-deficient patients.Immunohistochemical analysis and clinical aspects","author":"Barr\u03b9is","year":"1997","journal-title":"Acta Neuropathol"},{"key":"key-10.4103\/0028-3886.72164-33","first-page":"979","volume-title":"Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle","author":"Mizuno","year":"1994","journal-title":"Biochem Biophys Res Commun"},{"key":"key-10.4103\/0028-3886.72164-34","first-page":"202","volume-title":"Different manners of sarcoglycan expression in genetically proven a-sarcoglycan deficiency and g-sarcoglycan deficiency","author":"Higuchi","year":"1998","journal-title":"Acta Neuropathol"},{"key":"key-10.4103\/0028-3886.72164-35","first-page":"315","volume-title":"Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q","author":"Ben","year":"1992","journal-title":"Nat Genet"},{"key":"key-10.4103\/0028-3886.72164-36","first-page":"1449","volume-title":"Limb girdle muscular dystrophy.Description of a phenotype","author":"Stubjen","year":"1994","journal-title":"Muscle Nerve"},{"key":"key-10.4103\/0028-3886.72164-37","first-page":"1963","volume-title":"The sarcoglycan complex in the six autosomal recessive limbgirdle muscular dystrophies","author":"Vainzof","year":"1996","journal-title":"Hum Mol Genet"},{"key":"key-10.4103\/0028-3886.72164-38","first-page":"19","volume-title":"Population frequencies of inherited neuromuscular diseases: A world survey","author":"Emery","year":"1991","journal-title":"Neuromuscul Disord"},{"key":"key-10.4103\/0028-3886.72164-39","first-page":"392","volume-title":"The seven autosomal recessive limb-girdle muscular dystrophies (LGMD) in the Brazilian population from LGMD2A to LGMD2G","author":"Passos-Bueno","year":"1999","journal-title":"Am J Med Genet"},{"key":"key-10.4103\/0028-3886.72164-40","first-page":"71","volume-title":"Beta-Sarcoglycanopathy","author":"Kapoor","year":"2005","journal-title":"Indian J Pediatr"},{"key":"key-10.4103\/0028-3886.72164-41","first-page":"436","volume-title":"66th\/67th ENMC sponsored international workshop.The limb-girdle muscular dystrophies, 26-28 March 1999, Naarden, The Netherlands","author":"Beckmann","year":"1999","journal-title":"Neuromuscul Disord"},{"key":"key-10.4103\/0028-3886.72164-42","first-page":"473","volume-title":"Heart involvement in muscular dystrophies due to sarcoglycan gene mutations","author":"Melacini","year":"1999","journal-title":"Muscle Nerve"},{"key":"key-10.4103\/0028-3886.72164-43","first-page":"222","volume-title":"A biochemical, genetic and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey","author":"Dincer","year":"1997","journal-title":"Ann Neurol"},{"key":"key-10.4103\/0028-3886.72164-44","first-page":"379","volume-title":"Dysferlinopathy: A clinical and histopathological study of 28 patients from Southern India","author":"Nalini","year":"2008","journal-title":"Neurol India","ISSN":"https:\/\/id.crossref.org\/issn\/0028-3886","issn-type":"print"},{"key":"key-10.4103\/0028-3886.72164-45","first-page":"995","volume-title":"Limb-girdle muscular dystrophy in the United States","author":"Moore","year":"2006","journal-title":"J Neuropathol Exp Neurol"}],"container-title":["Neurology India"],"original-title":[],"language":"en","deposited":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T14:53:56Z","timestamp":1786632836000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/0028-3886.72164"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010]]},"references-count":45,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2010]]}},"alternative-id":["72164"],"URL":"https:\/\/doi.org\/10.4103\/0028-3886.72164","relation":{},"ISSN":["0028-3886"],"issn-type":[{"value":"0028-3886","type":"print"}],"subject":[],"published":{"date-parts":[[2010]]}}}