NEW Limb Girdle Muscular Dystrophy Type 2a by. BOOK (Paperback / softback)
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| Preise | 2013 | 2014 | 2015 | 2016 |
|---|---|---|---|---|
| Schnitt | Fr. 34.46 (€ 35.24)¹ | Fr. 35.75 (€ 36.56)¹ | Fr. 41.26 (€ 42.19)¹ | Fr. 53.68 (€ 54.90)¹ |
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Limb Girdle Muscular Dystrophy Type 2A
DE PB NWISBN: 9783659478314 bzw. 3659478318, in Deutsch, LAP LAMBERT Academic Publishing, Taschenbuch, neu.
Lieferung aus: Vereinigte Staaten von Amerika, Versandkosten nach: DEU.
Von Händler/Antiquariat, BuySomeBooks.
LAP LAMBERT Academic Publishing. Paperback. New. Paperback. 64 pages. Dimensions: 8.7in. x 5.9in. x 0.1in.ABSTRACT Limb girdle muscular dystrophy (LGMD) is a heterogeneous genetically determined group of skeletal muscle disorders. Among the 24 reported subtypes of LGMD, limb- girdle muscular dystrophy type 2A (LGMD2A) is caused by mutations in the calpain 3 (CAPN3) gene. In Pakistan, consanguineous marriages are common due to social, ethnic and traditional customs which is a leading cause of calpainopathy. In the present study, two families (A, B) showing clinically distinct autosomal recessive limb girdle muscular dystrophy type 2A were evaluated genetically. Any other abnormality was not observed in both families. Technique of homozygosity mapping was used to track the gene responsible for autosomal recessive LGMD2A in both families. In homozygosity mapping with polymorphic microsatellite markers, linkage in family A and B with LGMD2A was established to CAPN3 gene on chromosome 15q15. 1-q21. 1. Subsequently, sequence analysis of all 24 exons of CAPN3 was performed but no disease causing DNA sequence variant was found in these exons suggesting the presence of mutation in the regulatory sequences or any other genes present in this region. This item ships from multiple locations. Your book may arrive from Roseburg,OR, La Vergne,TN.
Von Händler/Antiquariat, BuySomeBooks.
LAP LAMBERT Academic Publishing. Paperback. New. Paperback. 64 pages. Dimensions: 8.7in. x 5.9in. x 0.1in.ABSTRACT Limb girdle muscular dystrophy (LGMD) is a heterogeneous genetically determined group of skeletal muscle disorders. Among the 24 reported subtypes of LGMD, limb- girdle muscular dystrophy type 2A (LGMD2A) is caused by mutations in the calpain 3 (CAPN3) gene. In Pakistan, consanguineous marriages are common due to social, ethnic and traditional customs which is a leading cause of calpainopathy. In the present study, two families (A, B) showing clinically distinct autosomal recessive limb girdle muscular dystrophy type 2A were evaluated genetically. Any other abnormality was not observed in both families. Technique of homozygosity mapping was used to track the gene responsible for autosomal recessive LGMD2A in both families. In homozygosity mapping with polymorphic microsatellite markers, linkage in family A and B with LGMD2A was established to CAPN3 gene on chromosome 15q15. 1-q21. 1. Subsequently, sequence analysis of all 24 exons of CAPN3 was performed but no disease causing DNA sequence variant was found in these exons suggesting the presence of mutation in the regulatory sequences or any other genes present in this region. This item ships from multiple locations. Your book may arrive from Roseburg,OR, La Vergne,TN.
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Limb Girdle Muscular Dystrophy Type 2a (2013)
DE PB NWISBN: 9783659478314 bzw. 3659478318, in Deutsch, Lap Lambert Academic Publishing, Taschenbuch, neu.
Lieferung aus: Niederlande, 5-10 werkdagen.
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Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
bol.com.
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
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Limb Girdle Muscular Dystrophy Type 2a by Khan Muhammad Jaseem Paperback Book (E
DE PB NWISBN: 9783659478314 bzw. 3659478318, in Deutsch, Taschenbuch, neu.
Lieferung aus: Vereinigte Staaten von Amerika, Lieferart: Free, Lieferung: Weltweit, Artikelstandort: 45014 Fairfield,OH,USA, Versandkostenfrei.
Von Händler/Antiquariat, grandeagleretail.
Festpreisangebot.
Von Händler/Antiquariat, grandeagleretail.
Festpreisangebot.
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NEW Limb Girdle Muscular Dystrophy Type 2a by. BOOK (Paperback / softback)
DE PB NWISBN: 9783659478314 bzw. 3659478318, in Deutsch, Taschenbuch, neu.
Lieferung aus: Vereinigte Staaten von Amerika, Lieferart: Free, Lieferung: Europe, Artikelstandort: USA, Versandkostenfrei.
Von Händler/Antiquariat, grey_elk_books_au_and_uk - Grey Elk Books.
Festpreisangebot.
Von Händler/Antiquariat, grey_elk_books_au_and_uk - Grey Elk Books.
Festpreisangebot.
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