scholarly article | Q13442814 |
P356 | DOI | 10.1002/(SICI)1097-4598(200005)23:5<818::AID-MUS23>3.0.CO;2-O |
P698 | PubMed publication ID | 10797409 |
P50 | author | Jan Senderek | Q30225211 |
P2093 | author name string | J M Schröder | |
Carsten Bergmann | |||
C Bergmann | |||
Anna Jauch | |||
Bart Janssen | |||
A Jauch | |||
B Janssen | |||
B Hermanns | |||
D Karch | |||
Benita Hermanns | |||
Jan Senderek | |||
Dieter Karch | |||
J. Michael Schr�der | |||
P2860 | cites work | Connexin mutations in X-linked Charcot-Marie-Tooth disease | Q24323296 |
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein | Q28118471 | ||
Population frequencies of inherited neuromuscular diseases—A world survey | Q28266298 | ||
Epidemiology of peripheral neuropathy | Q33735651 | ||
Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis | Q40310941 | ||
Charcot-Marie-Tooth neuropathies: from clinical description to molecular genetics | Q40601250 | ||
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus | Q42658269 | ||
The devastating combination of Charcot-Marie-Tooth disease and facioscapulohumeral muscular dystrophy | Q45111369 | ||
X-linked dominant Charcot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations(1). | Q48091038 | ||
Efficient neurophysiologic selection of X-linked Charcot-Marie-Tooth families: ten novel mutations | Q48349354 | ||
Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons | Q48833328 | ||
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a) | Q58183892 | ||
Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands | Q67737720 | ||
DNA duplication associated with Charcot-Marie-Tooth disease type 1A | Q68308484 | ||
A small deletion in the Duchenne/Becker muscular dystrophy locus--a functionally important region? | Q70191921 | ||
Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophy | Q72387813 | ||
[A new x-chromosomal muscular dystrophy] | Q73787710 | ||
P433 | issue | 5 | |
P921 | main subject | Becker muscular dystrophy | Q2484592 |
P304 | page(s) | 818-823 | |
P577 | publication date | 2000-05-01 | |
P1433 | published in | Muscle and Nerve | Q15764281 |
P1476 | title | Becker muscular dystrophy combined with x-linked Charcot-Marie-Tooth neuropathy | |
Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathy | |||
P478 | volume | 23 |