A case of hereditary inclusion body myopathy: 1 patient, 2 novel mutations. (Record no. 18531315)

MARC details
000 -LEADER
fixed length control field 00863 a2200229 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250515152107.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201210s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1537-1611
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1097/01.cnd.0000211406.94445.f0
Source of number or code doi
040 ## - CATALOGING SOURCE
Original cataloging agency NLM
Language of cataloging eng
Transcribing agency NLM
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Fisher, Justin
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20121002
245 00 - TITLE STATEMENT
Title A case of hereditary inclusion body myopathy: 1 patient, 2 novel mutations.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Journal of clinical neuromuscular disease
Date of publication, distribution, etc. Jun 2006
300 ## - PHYSICAL DESCRIPTION
Extent 179-84 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Towfighi, Javad
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Darvish, Daniel
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Simmons, Zachary
773 0# - HOST ITEM ENTRY
Title Journal of clinical neuromuscular disease
Related parts vol. 7
-- no. 4
-- p. 179-84
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1097/01.cnd.0000211406.94445.f0">https://doi.org/10.1097/01.cnd.0000211406.94445.f0</a>
Public note Available from publisher's website

No items available.