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Dysferlin also
known as dystrophy-****ociated fer-1-like
protein is a
protein that in
humans is
encoded by the DYSF gene.
Dysferlin is
linked with plasma...
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Mutation of many
different genes can be causative. Many
types involve dysferlin. All of the
different types affect different regions of the extremities...
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human dysferlin. The long form has six C2 domains.
Dysferlin and
myoferlin are
proteins found in
humans that are
homologous to otoferlin. Both
dysferlin and...
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mission of
which is to cure limb-girdle
muscular dystrophies caused by
dysferlin protein deficiency, a
condition that Jain's son has. List of
Jains Indians...
- accordingly.
Myoferlin and
dysferlin DysF
domains show 61%
sequence identity. A
unique feature of DysF
domains in both
dysferlin and
myoferlin is that these...
- biochemist. Thoms's
research areas are peroxisomes,
translational readthrough,
dysferlin, and rare
diseases caused by
defective cell organelles.
Thoms and colleagues...
- States, in
descending order, are
those due to
mutation of 1) calpain, 2)
dysferlin, 3)
collagen VI, 4) sarcoglycans, 5)
anoctamin 5, and 6) ****utin-related...
- D,
Miyake K,
Muniz VP,
Weiss RM,
McNeil PL,
Campbell KP (July 2007). "
Dysferlin-mediated
membrane repair protects the
heart from stress-induced left ventricular...
- REEP1, IGHMBP2, SLC5A7, DCTN1, TRPV4, SIGMAR1
Distal muscular dystrophy Dysferlin, TIA1, GNE (gene), MYH7, Titin, MYOT, MATR3,
unknown Dominant or recessive...
- D5
collagen 6-related LGMD R1 calpain3-related (Calpainopathy) LGMD R2
dysferlin-related LGMD R3 α-sarcoglycan-related LGMD R4 β-sarcoglycan-related LGMD...
