✦ LIBER ✦

Complementation studies in human and caprine β-mannosidosis

✍ Scribed by P. Hu; D. A. Wenger; O. P. van Diggelen; W. J. Kleijer

Book ID: 105314533
Publisher: Springer
Year: 1991
Tongue: English
Weight: 359 KB
Volume: 14
Category: Article
ISSN: 0141-8955
DOI: 10.1007/bf01804382

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Dysmyelinogenesis in caprine β-mannosido

Dysmyelinogenesis in caprine β-mannosidosis: Ultrastructural and morphometric studies in fetal optic nerve

✍ Lovell, Kathryn L.; Boyer, Philip J. 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 1018 KB

In Vitro Characterization of Oligodendro

In Vitro Characterization of Oligodendrocytes in Caprine β-Mannosidosis

✍ PHILIP J. BOYER; KATHRYN L. LOVELL 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 87 KB

Ultrastructural characteristics of the c

Ultrastructural characteristics of the cerebellum in caprine β-mannosidosis

✍ Kathryn L. Lovell; Margaret Z. Jones 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 78 KB

Regional Central Nervous System Oligosac

Regional Central Nervous System Oligosaccharide Storage in Caprine β-Mannosidosis

✍ Philip J. Boyer; Margaret Z. Jones; Eileen J. S. Rathke; Nancy K. Truscott; Kath 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 607 KB

Caprine β-Mannosidase: Sequencing and Ch

Caprine β-Mannosidase: Sequencing and Characterization of the cDNA and Identification of the Molecular Defect of Caprine β-Mannosidosis

✍ Jeffrey R. Leipprandt; Stacey A. Kraemer; Benjamin E. Haithcock; Hong Chen; Josh 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 253 KB

Investigation of dysmyelinogenesis in ca

Investigation of dysmyelinogenesis in caprine β-mannosidosis: In vitro characterization of oligodendrocytes

✍ Philip J. Boyer; Dr. Kathryn L. Lovell 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 716 KB

## Abstract Central nervous system myelin deficiency is a consistent feature of caprine β‐mannosidosis, and autosomal recessive neurovisceral lysosomal storage disease. To investigate the possibility of an intrinsic oligodendrocyte defect in β‐mannosidosis, oligodendrocyte‐enriched glial cultures f