TY  - GEN
AU  - Middleton,L T
AU  - Christodoulou,K
AU  - Deymeer,F
AU  - Serdaroglu,P
AU  - Ozdemir,C
AU  - al-Qudah,A K
AU  - al-Shehab,A
AU  - Mavromatis,I
AU  - Mylonas,I
AU  - Evoli,A
AU  - Tsingis,M
AU  - Zamba,E
AU  - Kyriallis,K
TI  - Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity
SN  - 0077-8923
PY  - 1998///0804
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 17
KW  - Electrodiagnosis
KW  - Female
KW  - Genes, Dominant
KW  - Genes, Recessive
KW  - Genetic Linkage
KW  - Genetic Variation
KW  - Humans
KW  - Lod Score
KW  - Male
KW  - Microsatellite Repeats
KW  - Middle Aged
KW  - Myasthenia Gravis
KW  - congenital
KW  - Pedigree
KW  - Receptors, Cholinergic
KW  - deficiency
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1749-6632.1998.tb10922.x
ER  -