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Phosphorylase kinase deficiency: Severe glycogen storage disease with evidence of autosomal recessive mode of inheritance

✍ Scribed by O. Søvik; Th. de Barsy; B. Maehle

No coin nor oath required. For personal study only.

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Glycogen storage disease confined to the

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Direct evidence of autosomal recessive i

✍ Y. Sasaki,Mikiro Iseki,Shinya Yamaguchi,Yoshihiro Kurosawa… 📂 Article 📅 1998 🏛 Springer 🌐 English ⚖ 148 KB