TY  - GEN
AU  - Lal,Dennis
AU  - Neubauer,Bernd A
AU  - Toliat,Mohammad R
AU  - Altmüller,Janine
AU  - Thiele,Holger
AU  - Nürnberg,Peter
AU  - Kamrath,Clemens
AU  - Schänzer,Anne
AU  - Sander,Thomas
AU  - Hahn,Andreas
AU  - Nothnagel,Michael
TI  - Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing
SN  - 1932-6203
PY  - 2016///0701
KW  - Adolescent
KW  - Child
KW  - Child, Preschool
KW  - Female
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Male
KW  - Muscle Proteins
KW  - genetics
KW  - Mutation
KW  - Myotonia Congenita
KW  - complications
KW  - Rare Diseases
KW  - Rickets, Hypophosphatemic
KW  - Selenoproteins
KW  - Sodium-Phosphate Cotransporter Proteins, Type IIc
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1371/journal.pone.0146040
ER  -