Becker muscular dystrophy combined with x-linked Charcot-Marie-Tooth neuropathy

scientific article published on 01 May 2000

Becker muscular dystrophy combined with x-linked Charcot-Marie-Tooth neuropathy is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/(SICI)1097-4598(200005)23:5<818::AID-MUS23>3.0.CO;2-O
P698PubMed publication ID10797409

P50authorJan SenderekQ30225211
P2093author name stringJ 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
P2860cites workConnexin mutations in X-linked Charcot-Marie-Tooth diseaseQ24323296
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal proteinQ28118471
Population frequencies of inherited neuromuscular diseases—A world surveyQ28266298
Epidemiology of peripheral neuropathyQ33735651
Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosisQ40310941
Charcot-Marie-Tooth neuropathies: from clinical description to molecular geneticsQ40601250
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locusQ42658269
The devastating combination of Charcot-Marie-Tooth disease and facioscapulohumeral muscular dystrophyQ45111369
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 mutationsQ48349354
Localization of dystrophin to postsynaptic regions of central nervous system cortical neuronsQ48833328
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 NetherlandsQ67737720
DNA duplication associated with Charcot-Marie-Tooth disease type 1AQ68308484
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 dystrophyQ72387813
[A new x-chromosomal muscular dystrophy]Q73787710
P433issue5
P921main subjectBecker muscular dystrophyQ2484592
P304page(s)818-823
P577publication date2000-05-01
P1433published inMuscle and NerveQ15764281
P1476titleBecker muscular dystrophy combined with x-linked Charcot-Marie-Tooth neuropathy
Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathy
P478volume23