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Immunohistological evidence for second or somatic mutations as the underlying cause of dystrophin expression by isolated fibres in Xp21 muscular dystrophy of Duchenne-type severity

✍ Scribed by Carina Wallgren-Pettersson; Bharat Jasani; Lyndon G. Rosser; Lazarus Pavlou Lazarou; Louise V.B. Nicholson; Angus Clarke


Book ID
118931781
Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
704 KB
Volume
118
Category
Article
ISSN
0022-510X

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