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Online Mendelian Inheritance in Man OMIM is a comprehensive authoritative compendium of human genes and genetic phenotypes that is freely available and updated Online Mendelian Inheritance in Man OMIM is a comprehensive authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily The full text
3454 Divided By 4
3454 Divided By 4
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24 diseases for NEB Gene From OMIM ClinVar GTR LOVD GeneCards DISEASES Novoseek and Orphanet click the icon to the left of a disorder to see descriptions Online Mendelian Inheritance in Man OMIM is a comprehensive authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily
More than 60 mutations in the NEB gene have been found to cause nemaline myopathy Some of these mutations change single protein building blocks amino acids in the nebulin protein or Online Mendelian Inheritance in Man OMIM is a comprehensive authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily
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This gene encodes nebulin a giant protein component of the cytoskeletal matrix that coexists with the thick and thin filaments within the sarcomeres of skeletal muscle Research activities on this disease The documents contained in this website are presented for information purposes only The material is in no way intended to replace professional medical
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https://www.orpha.net › de › disease › gene › NEB
Der Inhalt dieser Website ersetzt in keiner Weise eine professionelle Beratung oder Behandlung durch qualifizierte Fachleute Die vorliegenden Informationen d rfen nicht als Grundlage f r
https://www.omim.org › entry
Online Mendelian Inheritance in Man OMIM is a comprehensive authoritative compendium of human genes and genetic phenotypes that is freely available and updated
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3454 Divided By 4 - More than 60 mutations in the NEB gene have been found to cause nemaline myopathy Some of these mutations change single protein building blocks amino acids in the nebulin protein or
