✦ LIBER ✦

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33

✍ Scribed by E. LeGuern; A. Guilbot; M. Kessali; N. Ravise; J. Tassin; T. Maisonobe; D. Grid; A. Brice

Book ID: 117670870
Publisher: Elsevier Science
Year: 1997
Tongue: English
Weight: 265 KB
Volume: 7
Category: Article
ISSN: 0960-8966
DOI: 10.1016/s0960-8966(97)87322-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Locus for an Axonal Form of Autosomal

A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3

✍ Ahmed Bouhouche; Ali Benomar; Nazha Birouk; Angélique Mularoni; Farid Meggouh; J 📂 Article 📅 1999 🏛 American Society of Human Genetics 🌐 English ⚖ 423 KB

A Second Locus for an Axonal Form of Aut

A Second Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 19q13.3

✍ Alejandro Leal; Bernal Morera; Gerardo Del Valle; Dieter Heuss; Corinna Kayser; 📂 Article 📅 2001 🏛 American Society of Human Genetics 🌐 English ⚖ 149 KB

Linkage of a new locus for autosomal rec

Linkage of a new locus for autosomal recessive axonal form of Charcot–Marie–Tooth disease to chromosome 8q21.3

✍ C Barhoumi; R Amouri; C Ben Hamida; M Ben Hamida; S Machghoul; M Gueddiche; F He 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 346 KB

Clinical and electrophysiological charac

Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3

✍ Corinna Berghoff; Martin Berghoff; Alejandro Leal; Bernal Morera; Ramiro Barrant 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 97 KB

The human neuregulin-2 (NRG2) gene: clon

The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q

✍ H. Z. Ring; H. Chang; Angèle Guilbot; Alexis Brice; Eric LeGuern; Uta Francke 📂 Article 📅 1999 🏛 Springer 🌐 English ⚖ 228 KB

Mapping of a New Locus for Autosomal Rec

Mapping of a New Locus for Autosomal Recessive Demyelinating Charcot-Marie-Tooth Disease to 19q13.1-13.3 in a Large Consanguineous Lebanese Family: Exclusion of MAG as a Candidate Gene

✍ Valérie Delague; Corinne Bareil; Sylvie Tuffery; Patrice Bouvagnet; Eliane Choue 📂 Article 📅 2000 🏛 American Society of Human Genetics 🌐 English ⚖ 472 KB