A common presentation of a rare genetic disorder clinically mimicking primary myopathy

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	393-401
Number of pages	9
Journal	Adolescent Medicine: State of the Art Reviews
Volume	23
Issue number	2
Publication status	Published - Aug 2012
Externally published	Yes

Cite this

@article{a709dc84b8bc439a971d7881139f6470,

title = "A common presentation of a rare genetic disorder clinically mimicking primary myopathy",

author = "Wu, \{K. H.C.\} and Kohn, \{M. R.\} and A. Turner and Sillence, \{D. O.\}",

year = "2012",

month = aug,

language = "English",

volume = "23",

pages = "393--401",

journal = "Adolescent Medicine: State of the Art Reviews",

issn = "1934-4287",

publisher = "American Academy of Pediatrics",

number = "2",

}

TY - JOUR

T1 - A common presentation of a rare genetic disorder clinically mimicking primary myopathy

AU - Wu, K. H.C.

AU - Kohn, M. R.

AU - Turner, A.

AU - Sillence, D. O.

PY - 2012/8

Y1 - 2012/8

UR - https://www.scopus.com/pages/publications/84871877032

M3 - Article

C2 - 23162949

AN - SCOPUS:84871877032

SN - 1934-4287

VL - 23

SP - 393

EP - 401

JO - Adolescent Medicine: State of the Art Reviews

JF - Adolescent Medicine: State of the Art Reviews

IS - 2

ER -